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Guillain-Barré syndrome with severe demyelination mimicking axonopathy
Guillain-Barré syndrome with severe demyelination mimicking axonopathy
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Guillain-Barré syndrome with severe demyelination mimicking axonopathy

Bohlega, Saeed A. ; Stigsby, Bent ; Haider, A. ; McLean, Donald

Muscle & nerve, 1997-04, Vol.20 (4), p.514-516 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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2
Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience
Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience
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Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience

Bohlega, Saeed ; Abou Al-Shaar, Hussam ; Alkhairallah, Thamer ; Al-Ajlan, Fahad ; Hasan, Nael ; Alkahtani, Khalid

European neurology, 2015-01, Vol.74 (5-6), p.227-236 [Periódico revisado por pares]

Basel, Switzerland: S. Karger AG

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3
Mutations in the J domain of DNAJB6 cause dominant distal myopathy
Mutations in the J domain of DNAJB6 cause dominant distal myopathy
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Mutations in the J domain of DNAJB6 cause dominant distal myopathy

Palmio, Johanna ; Jonson, Per Harald ; Inoue, Michio ; Sarparanta, Jaakko ; Bengoechea, Rocio ; Savarese, Marco ; Vihola, Anna ; Jokela, Manu ; Nakagawa, Masanori ; Noguchi, Satoru ; Olivé, Montse ; Masingue, Marion ; Kerty, Emilia ; Hackman, Peter ; Weihl, Conrad C. ; Nishino, Ichizo ; Udd, Bjarne

Neuromuscular disorders : NMD, 2020-01, Vol.30 (1), p.38-46 [Periódico revisado por pares]

England: Elsevier B.V

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4
Parkinson's Disease in Saudi Patients: A Genetic Study
Parkinson's Disease in Saudi Patients: A Genetic Study
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Parkinson's Disease in Saudi Patients: A Genetic Study

Al-Mubarak, Bashayer R ; Bohlega, Saeed A ; Alkhairallah, Thamer S ; Magrashi, Amna I ; AlTurki, Maha I ; Khalil, Dania S ; AlAbdulaziz, Basma S ; Abou Al-Shaar, Hussam ; Mustafa, Abeer E ; Alyemni, Eman A ; Alsaffar, Bashayer A ; Tahir, Asma I ; Al Tassan, Nada A Cookson, Mark R.

PloS one, 2015-08, Vol.10 (8), p.e0135950-e0135950 [Periódico revisado por pares]

United States: Public Library of Science

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5
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family

Al-Shaar, Hussam Abou ; Qadi, Najeeb ; Ahmed, Mohammed ; Meyer, Brian F ; Bohlega, Saeed

Journal of the neurological sciences, 2016-08, Vol.367, p.239-243 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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6
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
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
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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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