Next-generation sequencing in childhood disorders by Schnekenberg, R, Schnekenberg, R, Németh, A, Németh, A, Németh, A

The genetics of primary dystonias and related disorders. by Németh, A

The synthesis of minds and molecules leads to potential therapy for pantothenate kinase-associated neurodegeneration. by Németh, A

The future of diagnostics in Cerebellar Ataxias by Nemeth, A

Examining undergraduate examinations. by Ellis, S, Nemeth, A

First record of the Zitting Cisticola (Cisticola juncidis Rafinesque, 1810) in Hungary. by Németh, Á., Vadász, Cs.

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Next-generation sequencing in childhood disorders. by Schnekenberg, R, Németh, A

Genetic testing in neurology by Harrison, V, Nemeth, A

Clinical and molecular genetics of primary dystonias. by Müller, U, Steinberger, D, Németh, A

Homozygous deletion in CDH3 and hypotrichosis with juvenile macular dystrophy. by Halford, S, Holt, R, Németh, A, Downes, S

A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degeneration. by Dunne, E, Hyman, N, Huson, S, Németh, A

Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene. by Worth, P, Dunne, E, Nemeth, A, Wood, N

On the rapid assessment of mechanical behavior of a prototype nickel-based superalloy using small-scale testing by Sulzer, S, Alabort, E, Németh, A, Roebuck, B, Reed, R

Cell-mediated immunity in pigeon breeders' lung: The effect of removal from antigen exposure by Johnson, M, Nemeth, A, Condez, A, Clarke, S, Poulter, L

Coats-type retinal telangiectasia in case of Kabuki make-up syndrome (Niikawa-Kuroki syndrome). by Anandan, M, Porter, N, Nemeth, A, Blair, E, Downes, S

Catastrophic visual loss in a patient with Friedreich ataxia. by Porter, N, Downes, S, Fratter, C, Anslow, P, Németh, A

Cell-mediated immunity in pigeon breeders' lung: the effect of removal from antigen exposure. by Johnson, M, Nemeth, A, Condez, A, Clarke, S, Poulter, L

Detection rate of pathogenic mutations in ABCA4 using direct sequencing: clinical and research implications. by Downes, S, Packham, E, Cranston, T, Clouston, P, Seller, A, Németh, A

Mutations in PKC gamma in a UK family with spinocerebellar ataxia by Talbot, K, Doran, G, Nemeth, A, Oliver, P, James, P

Klinefelter-like phenotype and primary infertility in a male with a paracentric Xq inversion. by Németh, A, Gallen, I, Crocker, M, Levy, E, Maher, E