Knowledge on rare diseases and orphan drugs

COVID-19 & Rare diseases logo

Rare Diseases Resources for Refugees/Displaced Persons

Homepage > Rare diseases > Encyclopaedia

Encyclopaedia

ALPHABETICAL LIST

0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Other search option(s)

Search by disease

VACTERL/VATER association
- Article for general public
  Deutsch (2020.pdf) - Soma e.V.
  
  Svenska (2016) - Socialstyrelsen
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Malformations ano-rectales isolées - Diagnostic et prise en charge de la naissance à lâge de 6 ans - PNDS
- Review article
  English (2011) - Orphanet J Rare Dis
Vaginal carcinoma
- Clinical practice guidelines
  Deutsch (2020) - AWMF
Valvular pulmonary stenosis
- Clinical practice guidelines
  Français (2021) Prise en charge de la grossesse chez les patientes avec une cardiopathie congénitale complexe - PNDS
  
  Deutsch (2018) - AWMF
Van den Ende-Gupta syndrome
- Anesthesia guidelines
  Deutsch (2011) - Orphananesthesia
  
  English (2019) - Orphananesthesia
  
  Español (2018) - Orphananesthesia
  
  Čeština (2019) - Orphananesthesia
  
  Português (2019) - Orphananesthesia
Van der Woude syndrome
- Anesthesia guidelines
  English (2022) Van der Woude syndrome - Orphananesthesia
  
  Español (2022) - Orphananesthesia
- Clinical genetics review
  English (2021) - GeneReviews
Variant ABeta2M amyloidosis
- Article for general public
  Français (2014) - SNFMI
Variant Creutzfeldt-Jakob disease
- Clinical practice guidelines
  Deutsch (2024) - AWMF
Variant of Guillain-Barré syndrome
- Clinical practice guidelines
  Deutsch (2019) - AWMF
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
Variegate porphyria
- Article for general public
  Svenska (2023) Akuta hepatiska porfyrier - Socialstyrelsen
- Emergency guidelines
  Français (2022) Crise de porphyrie hépatique aiguë (Porphyrie aiguë intermittente, porphyrie variegata, coproporphyrie héréditaire) - G2M
  
  Français (2016.pdf) Porphyrie hépatique aiguë - Orphanet Urgences
  
  Polski (2007.pdf) Ostre porfirie watrobowe, objawy nerwowo-trzewne - Orphanet Urgences
  
  English (2007.pdf) Acute hepatic porphyria neuro-visceral crisis - Orphanet Urgences
  
  Español (2007.pdf) Porfirias hepáticas agudas - Orphanet Urgences
  
  Italiano (2016.pdf) Porfiria epatica acuta - Orphanet Urgences
  
  Italiano (2007.pdf) Porfirie acute epatiche - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical genetics review
  English (2019) - GeneReviews
Vascular Ehlers-Danlos syndrome
- Article for general public
  Suomi (2014.pdf) - FPD RD Unit
  
  Svenska (2023) Ehlers-Danlos syndrom, vaskulär form (vEDS) - Socialstyrelsen
- Emergency guidelines
  Français (2017.pdf) Syndrome dEhlers-Danlos vasculaire (SEDv - SED de type IV) - Orphanet Urgences
  
  Polski (2009.pdf) Zespol Ehlersa i Danlosa typu IV - Orphanet Urgences
  
  Deutsch (2009.pdf) Ehlers-Danlos-Syndrom Typ IV - Orphanet Urgences
  
  English (2009.pdf) Type IV Ehlers-Danlos Syndrome - Orphanet Urgences
  
  Español (2009.pdf) Síndrome de Ehlers-Danlos de tipo IV - Orphanet Urgences
  
  Italiano (2009.pdf) Sindrome di Ehlers-Danlos tipo IV - Orphanet Urgences
  
  Português (2009.pdf) Síndrome de Ehlers-Danlos do tipo IV - Orphanet Urgences
- Anesthesia guidelines
  Deutsch (2019) - Orphananesthesia
  
  English (2019) - Orphananesthesia
  
  Español (2019) - Orphananesthesia
  
  Čeština (2019) - Orphananesthesia
- Clinical practice guidelines
  English (2018) Treatment of vascular Ehlers-Danlos syndrome: a systematic review - Ann Surg
  
  English (2018) Ehlers-Danlos syndromes: state of the art on clinical practice guidelines - RMD Open
  
  English (2022) Surveillance and monitoring in vascular Ehlers-Danlos syndrome in European Reference Network For Rare Vascular Diseases (VASCERN) - Eur J Med Genet
  
  English (2024) Guidelines for the management of peripheral arterial and aortic diseases: Developed by the task force on the management of peripheral arterial and aortic diseases of the European Society of Cardiology (ESC) - Eur Heart J
  
  English (2017) Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome - Am J Med Genet C Semin Med Genet
  
  English (2014) Recommendations for anesthesia and perioperative management in patients with Ehlers-Danlos syndrome(s) - Orphanet J Rare Dis
  
  English (2020) The Ehlers-Danlos syndromes - Nat Rev Dis Primers
  
  English (2018) Ehlers-Danlos syndromes: state of the art on clinical practice guidelines - RMD Open
  
  English (2023) HTAD patient pathway: Strategy for diagnostic work-up of patients and families with (suspected) heritable thoracic aortic diseases (HTAD). A statement from the HTAD working group of VASCERN - Eur J Med Genet
- Review article
  Français (2023) Le syndrome dEhlers Danlos : une maladie rare fréquemment suspectée - Bull Cancer
  
  English (2007) - Orphanet J Rare Dis
- Clinical genetics review
  English (2019) - GeneReviews
- Guidance for genetic testing
  English (2010) - Eur J Hum Genet
Vascular Ehlers-Danlos-polymicrogyria syndrome
- Review article
  Français (2023) Le syndrome dEhlers Danlos : une maladie rare fréquemment suspectée - Bull Cancer
Vasculitis
- Article for general public
  Norsk (2016) - PRINTO/PRES
  
  Français (2014) - SNFMI
  
  עברית (2016) - PRINTO/PRES
  
  Polski (2016) - PRINTO/PRES
  
  Latviešu (2016) - PRINTO/PRES
  
  Deutsch (2016) - PRINTO/PRES
  
  Українська (2016) - PRINTO/PRES
  
  Ελληνικά (2016) - PRINTO/PRES
  
  English (2016) - PRINTO/PRES
  
  Español (2016) - PRINTO/PRES
  
  Nederlands (2016) - PRINTO/PRES
  
  Türkçe (2016) - PRINTO/PRES
  
  ไทย (2016) - PRINTO/PRES
  
  বাংলা (2016) - PRINTO/PRES
  
  Slovenščina (2016) - PRINTO/PRES
  
  Slovenčina (2016) - PRINTO/PRES
  
  Dansk (2016) - PRINTO/PRES
  
  Српски (2016) - PRINTO/PRES
  
  Čeština (2016) - PRINTO/PRES
  
  Русский (2016) - PRINTO/PRES
  
  Hrvatski (2016) - PRINTO/PRES
  
  中文 (2016) - PRINTO/PRES
  
  Română (2016) - PRINTO/PRES
  
  Magyar (2016) - PRINTO/PRES
  
  Italiano (2016) - PRINTO/PRES
  
  العربية (2016) - PRINTO/PRES
  
  Português (2016) - PRINTO/PRES
- Emergency guidelines
  Français (2021.pdf) Vascularites nécrosantes systémiques - Orphanet Urgences
Vegetative pyoderma gangrenosum
- Clinical practice guidelines
  Deutsch (2020) - AWMF
Vein of Galen aneurysmal malformation
- Anesthesia guidelines
  English (2021) - Orphananesthesia
Vernal keratoconjunctivitis
- Clinical practice guidelines
  Français (2022) La kératoconjonctivite vernale KCV - PNDS
Verrucous hemangioma
- Article for general public
  English (2016) - PDQ Cancer Inf Sum
- Review article
  English (2017) - PDQ Cancer Inf Sum
Very long chain acyl-CoA dehydrogenase deficiency
- Article for general public
  Svenska (2024) - Socialstyrelsen
- Emergency guidelines
  Français (2023) Déficits oxydation acides gras : VLCAD, LCHAD, CPT2, Translocase, Trifonctionnelle, Acidurie Glutarique de type 2 (AG2) - G2M
  
  English (2023.pdf) Mitochondrial fatty acid ß-oxidation disorders - G2M
  
  English (2012.pdf) - Brit Inher Metab Dis Group
- Clinical practice guidelines
  Français (2021) Déficit en MCAD et autres déficits de la ?-oxydation mitochondriale des acides gras - PNDS
  
  English (2020) Nutrition management guideline for very-long chain acyl-CoA dehydrogenase deficiency (VLCAD): An evidence- and consensus-based approach - Mol Genet Metab
- Clinical genetics review
  English (2023) Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency - GeneReviews
Vestibular schwannoma
- Review article
  English (2021) Vestibular Schwannomas - N Engl J Med
VEXAS syndrome
- Clinical practice guidelines
  Français (2022) Greffe de cellules souches hématopoïétiques dans les maladies auto-immunes - PNDS
Vibratory urticaria
- Clinical practice guidelines
  Deutsch (2022) - AWMF
Vici syndrome
- Clinical practice guidelines
  Français (2022) Déficits immunitaires héréditaires - PNDS
  
  English (2020) European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management - J Clin Immunol
- Review article
  English (2016) Vici syndrome: a review - Orphanet J Rare Dis
- Clinical genetics review
  English (2022) EPG5-Related Disorder - GeneReviews
- Guidance for genetic testing
  English (2013) - Eur J Hum Genet
VIPoma
- Clinical practice guidelines
  English (2012) Guidelines for the management of gastroenteropancreatic neuroendocrine (including carcinoid) tumours (NETs) - Gut
- Review article
  English (2012) Pancreatic neuroendocrine tumors: clinical features, diagnosis and medical treatment: advances - Best Pract Res Clin Gastroenterol
Viral hemorrhagic fever
- Clinical practice guidelines
  Deutsch (2018) - AWMF
Vitamin B12-responsive methylmalonic acidemia
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
Vitamin B12-responsive methylmalonic acidemia type cblA
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
- Clinical genetics review
  English (2021) Disorders of Intracellular Cobalamin Metabolism - GeneReviews
  
  English (2022) - GeneReviews
Vitamin B12-responsive methylmalonic acidemia type cblB
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
- Clinical genetics review
  English (2021) Disorders of Intracellular Cobalamin Metabolism - GeneReviews
  
  English (2022) - GeneReviews
Vitamin B12-responsive methylmalonic acidemia, type cblDv2
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
Vitamin B12-unresponsive methylmalonic acidemia
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
- Clinical genetics review
  English (2022) - GeneReviews
Vitamin B12-unresponsive methylmalonic acidemia type mut-
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
- Clinical genetics review
  English (2022) - GeneReviews
Vitamin B12-unresponsive methylmalonic acidemia type mut0
- Article for general public
  Français (2011.pdf) - EIMD
  
  Polski (2011.pdf) - EIMD
  
  Deutsch (2011.pdf) - EIMD
  
  English (2011.pdf) - EIMD
  
  Español (2011.pdf) - EIMD
  
  Nederlands (2011.pdf) - EIMD
  
  Türkçe (2011.pdf) - EIMD
  
  Svenska (2021) - Socialstyrelsen
  
  Čeština (2011.pdf) - EIMD
  
  Hrvatski (2011.pdf) - EIMD
  
  Italiano (2011.pdf) - EIMD
  
  Português (2011.pdf) - EIMD
- Emergency guidelines
  English (2012.pdf) - Brit Inher Metab Dis Group
- Anesthesia guidelines
  English (2017) - Orphananesthesia
  
  Čeština (2017) - Orphananesthesia
- Clinical practice guidelines
  Français (2020) Aciduries organiques : Acidémie Méthylmalonique et Acidémie Propionique - PNDS
  
  English (2021) Guidelines for the diagnosis and management ofmethylmalonic acidaemia and propionic acidaemia - J Inherit Metab Dis
  
  English (2014) Proposed guidelines for the diagnosis and management of methylmalonic and propionic acidemia - Orphanet J Rare Dis
- Clinical genetics review
  English (2022) - GeneReviews
Vitreoretinopathy
- Article for general public
  Deutsch (2013.pdf) - ÄZQ
Vogt-Koyanagi-Harada disease
- Review article
  English (2016) Vogt-Koyanagi-Harada disease: review of a rare autoimmune disease targeting antigens of melanocytes - Orphanet J Rare Dis
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
- Diagnostic Keys
  Français (2023) Uvéite - Les clés du diagnostic
Von Hippel-Lindau disease
- Article for general public
  Deutsch (2017.pdf) - ACHSE
  
  Svenska (2017) - Socialstyrelsen
- Anesthesia guidelines
  Deutsch (2022) - Orphananesthesia
  
  English (2022) - Orphananesthesia
- Clinical practice guidelines
  English (2013) Von Hippel-Lindau disease (vHL). National clinical guideline for diagnosis and surveillance in Denmark. 3rd edition - Dan Med J
  
  English (2022) von Hippel-Lindau disease: Updated guideline for diagnosis and surveillance - Eur J Med Genet
  
  English (2020) Adrenocortical carcinomas and malignant phaeochromocytomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up - Ann Oncol
- Review article
  English (2014) - Oncol Res Treat
- Clinical genetics review
  English (2011) - Eur J Hum Genet
  
  English (2023) Von Hippel-Lindau Syndrome - GeneReviews
- Disability factsheet
  Dansk (2018) - Sjaeldne Diagnoser
- Guidance for genetic testing
  English (2013) - Eur J Hum Genet
Von Voss-Cherstvoy syndrome
- Anesthesia guidelines
  English (2013) - Orphananesthesia
  
  Čeština (2013) - Orphananesthesia
Von Willebrand disease
- Article for general public
  Français (2006.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Disability factsheet
  Dansk (2018) - Sjaeldne Diagnoser
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
- Guidance for genetic testing
  Français (2015.pdf) - ANPGM
  
  English (2011) - Eur J Hum Genet
Von Willebrand disease type 1
- Article for general public
  Français (2009.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
- Guidance for genetic testing
  Français (2015.pdf) - ANPGM
Von Willebrand disease type 2
- Article for general public
  Français (2009.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
- Guidance for genetic testing
  Français (2015.pdf) - ANPGM
Von Willebrand disease type 2A
- Article for general public
  Français (2009.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) von Willebrand Disease - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
Von Willebrand disease type 2B
- Article for general public
  Français (2009.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
Von Willebrand disease type 2M
- Article for general public
  Français (2009.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
Von Willebrand disease type 2N
- Article for general public
  Français (2009.pdf) - Orphanet
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
Von Willebrand disease type 3
- Article for general public
  Français (2009.pdf) - Orphanet
  
  Svenska (2023) - Socialstyrelsen
- Emergency guidelines
  Français (2019.pdf) Maladie de von Willebrand - Orphanet Urgences
- Anesthesia guidelines
  English (2014) - Orphananesthesia
  
  Español (2014) - Orphananesthesia
  
  Čeština (2014) - Orphananesthesia
- Clinical practice guidelines
  Français (2021) Maladie de Willebrand - PNDS
  
  Français (2022) Saignements Utérins Abondants (SUA) chez la jeune femme atteinte de maladies hémorragiques rares constitutionnelles ou acquises (MHCA) - PNDS
  
  Français (2021) Maladie de Willebrand type 3 - PNDS
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Blood Adv
  
  English (2021) ASH ISTH NHF WFH 2021 guidelines on the management of von Willebrand disease - Blood Adv
  
  中文 (2021) ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease - Zhonghua Xue Ye Xue Za Zhi
- Clinical genetics review
  English (2017) - GeneReviews
- Patient-Centered Outcome Measures (PCOMs)
  English (2023) - PROQOLID^TM
- Guidance for genetic testing
  Français (2015.pdf) - ANPGM
Vulvar intraepithelial neoplasia
- Article for general public
  Deutsch (2019) - VulvaKarzinom-SHG
- Clinical practice guidelines
  Deutsch (2015) - AWMF
Vulvovaginal rhabdomyosarcoma
- Clinical practice guidelines
  Deutsch (2020) - AWMF