Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 21 for Netherlands
  1. Frontotemporal dementia with parkinsonism-17 
    ... prevalence of FTDP-17 is unknown. In the Netherlands, where the disease prevalence has been studied, it ... P, van Swieten JC. Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population- ...
    https://medlineplus.gov/...ntotemporal-dementia-with-parkinsonism-17 - Genetics
  2. Multiminicore disease 
    ... MmD Workshop, 9-11 November 2002, Naarden, The Netherlands. Neuromuscul Disord. 2004 Nov;14(11):754-66. ...
    https://medlineplus.gov/genetics/condition/multiminicore-disease - Genetics
  3. Facioscapulohumeral muscular dystrophy 
    ... dystrophy: workshop 9th June 2010, LUMC, Leiden, The Netherlands. Neuromuscul Disord. 2012 May;22(5):463-70. ...
    https://medlineplus.gov/.../facioscapulohumeral-muscular-dystrophy - Genetics
  4. Trichorhinophalangeal syndrome type I 
    ... rare condition; its prevalence is unknown. In the Netherlands, at least 35 people have TRPS I. TRPS ...
    https://medlineplus.gov/.../trichorhinophalangeal-syndrome-type-i - Genetics
  5. TPO gene 
    ... decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects ( ...
    https://medlineplus.gov/genetics/gene/tpo - Genetics
  6. TNNT2 gene 
    ... Tintelen JP. Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated ...
    https://medlineplus.gov/genetics/gene/tnnt2 - Genetics
  7. Wagner syndrome 
    ... about half of these individuals are from the Netherlands. Mutations in the VCAN gene cause Wagner syndrome. ...
    https://medlineplus.gov/genetics/condition/wagner-syndrome - Genetics
  8. SMPD1 gene 
    ... BJ. Acid sphingomyelinase (Asm) deficiency patients in The Netherlands and Belgium: disease spectrum and natural course in ...
    https://medlineplus.gov/genetics/gene/smpd1 - Genetics
  9. Spinal muscular atrophy with respiratory distress type 1 
    ... type 1: 11-13 May 2012, Naarden, The Netherlands. Neuromuscul Disord. 2013 Jul;23(7):602-9. ...
    https://medlineplus.gov/...-atrophy-with-respiratory-distress-type-1 - Genetics
  10. TFR2 gene 
    ... NM, Swinkels DW. TFR2-related haemochromatosis in the Netherlands: a cause of arthralgia in young adulthood. Neth ...
    https://medlineplus.gov/genetics/gene/tfr2 - Genetics
previous · 1 · 2 · 3 · next