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Refinado por: assunto: Adult remover assunto: Medical Sciences remover
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1
Cyclosporine-induced migraine with severe vomiting causing loss of renal graft
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Artigo
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Cyclosporine-induced migraine with severe vomiting causing loss of renal graft

Maghrabi, Khalid ; Bohlega, Saeed

Clinical neurology and neurosurgery, 1998-09, Vol.100 (3), p.224-227 [Periódico revisado por pares]

Amsterdam: Elsevier B.V

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2
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula
Material Type:
Artigo
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Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula

Bohlega, Saeed ; Al-Jishi, Adel ; Dobson-Stone, Carol ; Rampoldi, Luca ; Saha, Parthasarathi ; Murad, Hatem ; Kareem, Abid ; Roberts, George ; Monaco, Anthony P.

Movement disorders, 2003-04, Vol.18 (4), p.403-407 [Periódico revisado por pares]

New York: Wiley Subscription Services, Inc., A Wiley Company

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3
Neurological complications in liver transplantation
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Artigo
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Neurological complications in liver transplantation

GHAUS, Naveed ; BOHLEGA, Saeed ; REZEIG, Mohammed

Journal of neurology, 2001-12, Vol.248 (12), p.1042-1048 [Periódico revisado por pares]

Berlin: Springer

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4
Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1
Material Type:
Artigo
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Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1

Al-Semari, Abdulaziz ; Bohlega, Saeed

American journal of medical genetics. Part A, 2007-01, Vol.143A (2), p.149-160 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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5
Neurobrucellosis: Clinical and neuroimaging correlation
Material Type:
Artigo
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Neurobrucellosis: Clinical and neuroimaging correlation

AL-SOUS, M. Walid ; BOHLEGA, Saeed ; AL-KAWI, M. Zuheir ; ALWATBAN, Jehad ; MCLEAN, Donald R

American journal of neuroradiology : AJNR, 2004-03, Vol.25 (3), p.395-401 [Periódico revisado por pares]

Oak Brook, IL: American Society of Neuroradiology

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6
Genotype–phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype
Material Type:
Artigo
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Genotype–phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype

Ganesh, Subramaniam ; Delgado-Escueta, Antonio V. ; Suzuki, Toshimitsu ; Francheschetti, Silvana ; Riggio, Concetta ; Avanzini, Giuiliano ; Rabinowicz, Adrian ; Bohlega, Saeed ; Bailey, Julia ; Alonso, Maria E. ; Rasmussen, Astrid ; Thomson, Alfredo E. ; Ochoa, Adriana ; Prado, Aurelio J. ; Medina, Marco T. ; Yamakawa, Kazuhiro

Human molecular genetics, 2002-05, Vol.11 (11), p.1263-1271 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegia
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Artigo
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Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegia

Khan, S ; Yaqub, B A ; Poser, C M ; al Deeb, S M ; Bohlega, S

Journal of neurology, neurosurgery and psychiatry, 1995-04, Vol.58 (4), p.467-470 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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8
Transcranial magnetic stimulation in Behçet's disease: a cross-sectional and longitudinal study with 44 patients comparing clinical, neuroradiological, somatosensory and brain-stem auditory evoked potential findings
Material Type:
Artigo
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Transcranial magnetic stimulation in Behçet's disease: a cross-sectional and longitudinal study with 44 patients comparing clinical, neuroradiological, somatosensory and brain-stem auditory evoked potential findings

Stigsby, Bent ; Bohlega, Saeed ; McLean, Donald R ; Al-Kawi, Mohammed Zuheir

Clinical neurophysiology, 2000-07, Vol.111 (7), p.1320-1329 [Periódico revisado por pares]

Shannon: Elsevier Ireland Ltd

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9
T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease
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Artigo
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T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease

Chishti, Muhammad A ; Bohlega, Saeed ; Ahmed, Maqbool ; Loualich, Arslan ; Carroll, Pamela ; Sato, Christine ; St George-Hyslop, Peter ; Westaway, David ; Rogaeva, Ekaterina

Archives of neurology (Chicago), 2006-10, Vol.63 (10), p.1483-1485

Chicago, IL: American Medical Association

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10
Behçet's disease and the nervous system
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Artigo
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Behçet's disease and the nervous system

SERDAROGLU, P

Journal of neurology, 1998-04, Vol.245 (4), p.197-205 [Periódico revisado por pares]

Berlin: Springer

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