Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1AL-SEMARI, Abdulaziz; BOHLEGA, Saeed.American journal of medical genetics. Part A. 2007, Vol 143, Num 2, pp 149-160, issn 1552-4825, 12 p.Article

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in ArabsBOHLEGA, Saeed A; ABU-AMERO, Khaled K.Saudi medical journal. 2008, Vol 29, Num 7, pp 952-956, issn 0379-5284, 5 p.Article

Loss of ERLIN2 Function Leads to Juvenile Primary Lateral SclerosisAL-SAIF, Amr; BOHLEGA, Saeed; AL-MOHANNA, Futwan et al.Annals of neurology. 2012, Vol 72, Num 4, pp 510-516, issn 0364-5134, 7 p.Article

A Mutation in Sigma-1 Receptor Causes Juvenile Amyotrophic Lateral SclerosisAL-SAIF, Amr; AL-MOHANNA, Futwan; BOHLEGA, Saeed et al.Annals of neurology. 2011, Vol 70, Num 6, pp 913-919, issn 0364-5134, 7 p.Article

Neurological complications in liver transplantationGHAUS, Naveed; BOHLEGA, Saeed; REZEIG, Mohammed et al.Journal of neurology. 2001, Vol 248, Num 12, pp 1042-1048, issn 0340-5354Article

Neurodegenerative huntington-like disorderBOHLEGA, Saeed; AL-TAHAN, Abdulrahman; KAMBOURIS, Marios et al.Movement disorders. 2001, Vol 16, Num 3, pp 533-534, issn 0885-3185Article

T313M PINK1 mutation in an extended highly consanguineous saudi family with early-onset parkinson diseaseCHISHTI, Muhammad A; BOHLEGA, Saeed; AHMED, Maqbool et al.Archives of neurology (Chicago). 2006, Vol 63, Num 10, pp 1483-1485, issn 0003-9942, 3 p.Article

Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extra pyramidal SyndromeALAZAMI, Anas M; AL-SAIF, Amr; BALTUS, Andy et al.American journal of human genetics. 2008, Vol 83, Num 6, pp 684-691, issn 0002-9297, 8 p.Article

Chorea-acanthocytosis: Clinical and genetic findings in three families from the arabian peninsulaBOHLEGA, Saeed; AL-JISHI, Adel; DOBSON-STONE, Carol et al.Movement disorders. 2003, Vol 18, Num 4, pp 403-407, issn 0885-3185, 5 p.Article

Neurobrucellosis: Clinical and neuroimaging correlationAL-SOUS, M. Walid; BOHLEGA, Saeed; AL-KAWI, M. Zuheir et al.American journal of neuroradiology. 2004, Vol 25, Num 3, pp 395-401, issn 0195-6108, 7 p.Article

Mutations in NHLRC1 cause progressive myoclonus epilepsyCHAN, Elayne M; YOUNG, Edwin J; BOHLEGA, Saeed et al.Nature genetics. 2003, Vol 35, Num 2, pp 125-127, issn 1061-4036, 3 p.Article

Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotypeGANESH, Subramaniam; DELGADO-ESCUETA, Antonio V; RASMUSSEN, Astrid et al.Human molecular genetics (Print). 2002, Vol 11, Num 11, pp 1263-1271, issn 0964-6906Article

Primary Sjögren's syndrome with central nervous system involvementALHOMOUD, Iftetah A; BOHLEGA, Saeed A; ALKAWI, Mohammed Z et al.Saudi medical journal. 2009, Vol 30, Num 8, pp 1067-1072, issn 0379-5284, 6 p.Article

Pitfalls in cerebrospinal fluid test for the diagnosis of neurosyphilisAL-SEMARI, Abdulaziz M; BOHLEGA, Saeed I; CUPLER, Edward J et al.Saudi medical journal. 2001, Vol 22, Num 1, pp 26-29, issn 0379-5284Article