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Search Results - Ishpekova, Boryana
Search Results - Ishpekova, Boryana
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Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy
by
Thomas, Florian P.
,
Guergueltcheva, Velina
,
Gondim, Francisco A. A.
,
Tournev, Ivailo
,
Rao, Chitharanjan V.
,
Ishpekova, Boryana
,
Kinsella, Laurence J.
,
Pan, Yi
,
Geller, Thomas J.
,
Litvinenko, Ivan
,
De Jonghe, Peter
,
Scherer, Steven S.
,
Jordanova, Albena
Published in
Journal of neurology
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Hereditary motor and sensory neuropathy-Lom, a novel demyelinating neuropathy associated with deafness in gypsies: Clinical, electrophysiological and nerve biopsy findings
by
KALAYDJIEVA, L
,
NIKOLOVA, A
,
MERLINI, L
,
TROGU, A
,
MUDDLE, J. R
,
KING, R. H. M
,
THOMAS, P. K
,
TURNEV, I
,
PETROVA, J
,
HRISTOVA, A
,
ISHPEKOVA, B
,
PETKOVA, I
,
SHMAROV, A
,
STANCHEVA, S
,
MIDDLETON, L
Published in
Brain (London, England : 1878)
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Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease
by
Hunter, Michael
,
Bernard, Rafaëlle
,
Freitas, Elizabeth
,
Boyer, Amandine
,
Morar, Bharti
,
Martins, Ian J.
,
Tournev, Ivailo
,
Jordanova, Albena
,
Guergelcheva, Velina
,
Ishpekova, Boryana
,
Kremensky, Ivo
,
Nicholson, Garth
,
Schlotter, Beate
,
Lochmüller, Hanns
,
Voit, Thomas
,
Colomer, Jaume
,
Thomas, P.K.
,
Levy, Nicolas
,
Kalaydjieva, Luba
Published in
Human mutation
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Early Clinical and Electrophysiologic Features of the Two Most Common Autosomal Recessive Forms of Charcot-Marie-Tooth Disease in the Roma (Gypsies)
by
Guergueltcheva, Velina
,
Tournev, Ivailo
,
Bojinova, Veneta
,
Hantke, Janina
,
Litvinenko, Ivan
,
Ishpekova, Boryana
,
Shmarov, Alexander
,
Petrova, Julia
,
Jordanova, Albena
,
Kalaydjieva, Luba
Published in
Journal of child neurology
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Congenital cataracts facial dysmorphism neuropathy syndrome, a novel complex genetic disease in Balkan gypsies: Clinical and electrophysiological observations
by
Tournev, Ivailo
,
Kalaydjieva, Luba
,
Youl, Bryan
,
Ishpekova, Boryana
,
Guergueltcheva, Velina
,
Kamenov, Ognian
,
Katzarova, Maria
,
Kamenov, Zdravko
,
Raicheva-Terzieva, Margarita
,
King, R. H. M.
,
Romanski, Kiril
,
Petkov, Radoslav
,
Schmarov, Alexander
,
Dimitrova, Galina
,
Popova, Nevena
,
Uzunova, Maria
,
Milanov, Stephen
,
Petrova, Julia
,
Petkov, Yanko
,
Kolarov, Georgi
,
Aneva, Lidia
,
Radeva, Olia
,
Thomas, P. K.
Published in
Annals of neurology
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Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease: MUTATION SCREENING OF NDRG1 IN CMT DISEASE
by
Hunter, Michael
,
Bernard, Rafaëlle
,
Freitas, Elizabeth
,
Boyer, Amandine
,
Morar, Bharti
,
Martins, Ian J.
,
Tournev, Ivailo
,
Jordanova, Albena
,
Guergelcheva, Velina
,
Ishpekova, Boryana
,
Kremensky, Ivo
,
Nicholson, Garth
,
Schlotter, Beate
,
Lochmüller, Hanns
,
Voit, Thomas
,
Colomer, Jaume
,
Thomas, P.K.
,
Levy, Nicolas
,
Kalaydjieva, Luba
Published in
Human mutation
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Hereditary motor and sensory neuropathy – Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries
by
Chandler, David
,
Angelicheva, Dora
,
Heather, Lisa
,
Gooding, Rebecca
,
Gresham, David
,
Yanakiev, Peter
,
de Jonge, Roos
,
Baas, Frank
,
Dye, Danielle
,
Karagyozov, Luchezar
,
Savov, Alexei
,
Blechschmidt, Karin
,
Keats, Bronya
,
Thomas, P.K.
,
King, Rosalind H.M.
,
Starr, Arnold
,
Nikolova, Amelia
,
Colomer, Jaume
,
Ishpekova, Boryana
,
Tournev, Ivailo
,
Andoni Urtizberea, Jon
,
Merlini, Luciano
,
Butinar, Dusan
,
Chabrol, Brigitte
,
Voit, Thomas
,
Baethmann, Martina
,
Nedkova, Vania
,
Corches, Axinia
,
Kalaydjieva, Luba
Published in
Neuromuscular disorders : NMD
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