Congenital cataract, facial dysmorphism and demyelinating neuropathy (CCFDN) in 10 Czech gypsy children – frequent and underestimated cause of disability among Czech gypsies

[1]  L. Kalaydjieva,et al.  Congenital Cataracts, Facial Dysmorphism, and Neuropathy , 2014 .

[2]  R. Ádány,et al.  Policies to improve the health and well-being of Roma people: the European experience. , 2012, Health policy.

[3]  R. Zetter,et al.  Romani Mobilities in Europe: Multidisciplinary Perspectives , 2010 .

[4]  L. Kalaydjieva,et al.  Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a rare cause of parainfectious rhabdomyolysis , 2007, European Journal of Pediatrics.

[5]  L. Kalaydjieva.  Congenital Cataracts – Facial Dysmorphism – Neuropathy , 2006, Orphanet journal of rare diseases.

[6]  J. Lebl,et al.  Kazuistiky z molekulární genetiky , 2006 .

[7]  Dana Šišková.  Hereditární neuropatie s kongenitální kataraktou a faciální dysmorfií , 2005 .

[8]  F. Baas,et al.  125th ENMC International Workshop: Neuromuscular Disorders in the Roma (Gypsy) Population, 23–25 April 2004, Naarden, The Netherlands , 2005, Neuromuscular Disorders.

[9]  Jeff P. Reeve,et al.  Mutation history of the roma/gypsies. , 2004, American journal of human genetics.

[10]  Hanns Lochmüller,et al.  Ocular features of the congenital cataracts facial dysmorphism neuropathy syndrome. , 2004, Ophthalmology.

[11]  K. K. Yong,et al.  Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome , 2003, Nature Genetics.

[12]  D. Gresham,et al.  Genetic studies of the Roma (Gypsies): a review , 2001, BMC Medical Genetics.

[13]  Martin J. McKee,et al.  The health of the Roma people: a review of the published literature , 2000, Journal of epidemiology and community health.

[14]  L. Kalaydjieva,et al.  Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan gypsies: Clinical and electrophysiological observations , 1999, Annals of neurology.