Cyclosporine-induced migraine with severe vomiting causing loss of renal graftMAGHRABI, K; BOHLEGA, S.Clinical neurology and neurosurgery. 1998, Vol 100, Num 3, pp 224-227, issn 0303-8467Article

Acute sensory neuronopathy with preserved SEPs and long-latency reflexesKNAZAN, M; BOHLEGA, S; BERRY, K et al.Muscle & nerve. 1990, Vol 13, Num 5, pp 381-384, issn 0148-639X, 4 p.Article

The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxiaLORENZETTI, D; BOHLEGA, S; ZOGHBI, H. Y et al.Neurology. 1997, Vol 49, Num 4, pp 1009-1013, issn 0028-3878Article

Consensus guidelines for the diagnosis and treatment of multiple sclerosisYAMOUT, B; ALROUGHANI, R; EIKALLAB, K et al.Current medical research and opinion. 2013, Vol 29, Num 6, pp 611-621, issn 0300-7995, 11 p.Article

Gaucher disease with oculomotor apraxia and cardiovascular calcification (Gaucher type IIIC)BOHLEGA, S; KAMBOURIS, M; SHAHID, M et al.Neurology. 2000, Vol 54, Num 1, pp 261-263, issn 0028-3878Article

Localization of the gene for a novel autosomal recessive neurodegenerative Huntington-like disorder to 4p15.3KAMBOURIS, M; BOHLEGA, S; AL-TAHAN, A et al.American journal of human genetics. 2000, Vol 66, Num 2, pp 445-452, issn 0002-9297Article

Neuroacanthocytosis and aprebetalipoproteinemiaBOHLEGA, S; RILEY, W; POWE, J et al.Neurology. 1998, Vol 50, Num 6, pp 1912-1914, issn 0028-3878Article

Novel mutations in spastin gene and absence of correlation with age at onset of symptomsHENTATI, A; DENG, H.-X; LAING, N. G et al.Neurology. 2000, Vol 55, Num 9, pp 1388-1390, issn 0028-3878Article

A novel autosomal recessive Huntington's disease-like neurodegenerative disorder in a Saudi familyAL-TAHAN, A. Y; DIVAKARAN, M. P; KAMBOURIS, M et al.Saudi medical journal. 1999, Vol 20, Num 1, pp 85-89, issn 0379-5284Article

Multiple mitocondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathyBOHLEGA, S; TANJI, K; SANTORELLI, F. M et al.Neurology. 1996, Vol 46, Num 5, pp 1329-1334, issn 0028-3878Article

Skin biopsy in Lafora disease: Genotype-phenotype correlations and diagnostic pitfallsANDRADE, D. M; ACKERLEY, C. A; MINETT, T. S. C et al.Neurology. 2003, Vol 61, Num 11, pp 1611-1614, issn 0028-3878, 4 p.Article

Cerebral manifestation of Erdheim-Chester disease : Clinical and radiologic findingsBOHLEGA, S; ALWATBAN, J; TULBAH, A et al.Neurology. 1997, Vol 49, Num 6, pp 1702-1705, issn 0028-3878Article

Subacute sclerosing panencephalitis : Evaluation with CT and MRBRISMAR, J; GASCON, G. G; VON STEYERN, K. V et al.American journal of neuroradiology. 1996, Vol 17, Num 4, pp 761-772, issn 0195-6108Article

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markersHENTATI, A; PERICAK-VANCE, M. A; IQBAL, Z et al.Human molecular genetics (Print). 1994, Vol 3, Num 10, pp 1867-1871, issn 0964-6906Article

A novel syndromic form of sensory-motor polyneuropathy is linked to chromosome 22q13.31-q13.33BOHLEGA, S; ALAZAMI, A. M; CUPLER, E et al.Clinical genetics. 2011, Vol 79, Num 2, pp 193-195, issn 0009-9163, 3 p.Article

Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathyAOKI, M; LIU, J; BELEY, C et al.Neurology. 2001, Vol 57, Num 2, pp 271-278, issn 0028-3878Article

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyJING LIU; AOKI, M; BOHLEGA, S et al.Nature genetics. 1998, Vol 20, Num 1, pp 31-36, issn 1061-4036Article

Molecular and clinical studies in SCA-7 define a broad clinical spectrum and the infantile phenotypeBENTON, C. S; DE SILVA, R; RUTLEDGE, S. L et al.Neurology. 1998, Vol 51, Num 4, pp 1081-1086, issn 0028-3878Article

Huntington's disease : report on four Saudi familiesBOHLEGA, S; MCLEAN, D; AL KAWI, M. Z et al.Saudi medical journal. 1996, Vol 17, Num 4, pp 456-460, issn 0379-5284Article

Familial tremulous and myoclonic dystonia with white matter changes in brain magnetic resonance imagingBOHLEGA, S; STIGSBY, B; AL-KAWI, M. Z et al.Movement disorders. 1995, Vol 10, Num 4, pp 513-517, issn 0885-3185Article

Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegiaKHAN, S; YAQUB, B. A; POSER, C. M et al.Journal of neurology, neurosurgery and psychiatry. 1995, Vol 58, Num 4, pp 467-470, issn 0022-3050Article

Liposomal amphotericin B treatment of aspergillosis in a renal transplant patientELLIS, M. E; BOHLEGA, S; HALIM, M. A et al.Saudi medical journal. 1993, Vol 14, Num 5, pp 469-470, issn 0379-5284Article