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Treatment optimization in multiple sclerosis: report of an international consensus meeting
Treatment optimization in multiple sclerosis: report of an international consensus meeting
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Treatment optimization in multiple sclerosis: report of an international consensus meeting

International Working Group for Treatment Optimization in MS

European journal of neurology, 2004-01, Vol.11 (1), p.43-47 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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2
Neurobrucellosis: Clinical and neuroimaging correlation
Neurobrucellosis: Clinical and neuroimaging correlation
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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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3
The Burden of Musculoskeletal Conditions at the Start of the New MillenniumReport of a WHO Scientific Group. 2004, 218 pages. World Health Organization, Technical Report Series, No. 919, ISBN 92 4 120919 4
The Burden of Musculoskeletal Conditions at the Start of the New MillenniumReport of a WHO Scientific Group. 2004, 218 pages. World Health Organization, Technical Report Series, No. 919, ISBN 92 4 120919 4
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The Burden of Musculoskeletal Conditions at the Start of the New MillenniumReport of a WHO Scientific Group. 2004, 218 pages. World Health Organization, Technical Report Series, No. 919, ISBN 92 4 120919 4

Bohlega, Saeed

Annals of Saudi medicine, 2004-09, Vol.24 (5), p.403-404 [Periódico revisado por pares]

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4
Mitochondrial T9957C Mutation in Association with NAION and Seizures but not MELAS
Mitochondrial T9957C Mutation in Association with NAION and Seizures but not MELAS
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Mitochondrial T9957C Mutation in Association with NAION and Seizures but not MELAS

Abu-Amero, Khaled K. ; Bosley, Thomas M. ; Bohlega, Saeed ; Hansen, Erik

Ophthalmic genetics, 2005-03, Vol.26 (1), p.31-36 [Periódico revisado por pares]

England: Informa UK Ltd

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5
Unilateral pallidotomy for hemidystonia
Unilateral pallidotomy for hemidystonia
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Unilateral pallidotomy for hemidystonia

Alkhani, Ahmed ; Bohlega, Saeed

Movement disorders, 2006-06, Vol.21 (6), p.852-855 [Periódico revisado por pares]

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

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6
T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease
T313M PINK1 Mutation in an Extended Highly Consanguineous Saudi Family With Early-Onset Parkinson Disease
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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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7
Autosomal-recessive syndrome with alopecia, hypadism, progressive extra- pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1
Autosomal-recessive syndrome with alopecia, hypadism, progressive extra- pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1
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Autosomal-recessive syndrome with alopecia, hypadism, 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]

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8
Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1
Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1
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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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9
Integrating an evidence-based assessment of benefit and risk in disease-modifying treatment of multiple sclerosis
Integrating an evidence-based assessment of benefit and risk in disease-modifying treatment of multiple sclerosis
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Integrating an evidence-based assessment of benefit and risk in disease-modifying treatment of multiple sclerosis

Goodin, Douglas S. ; Biermann, Louis D. ; Bohlega, Saeed ; Boiko, Alexey ; Chofflon, Michel ; Gebeily, Souheil ; Gouider, Riadh ; Havrdova, Eva ; Jakab, Gabor ; Karabudak, Rana ; Karussis, Dimitrios ; Miller, Ariel ; Pakdaman, Hossein ; Selmaj, Krzysztof ; Sharief, Mohammad

Current medical research and opinion, 2007-11, Vol.23 (11), p.2823-2832 [Periódico revisado por pares]

England: Informa UK Ltd

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10
CADASIL in Arabs: clinical and genetic findings
CADASIL in Arabs: clinical and genetic findings
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CADASIL in Arabs: clinical and genetic findings

Bohlega, Saeed ; Al Shubili, Asmahan ; Edris, Abdulrahman ; Alreshaid, Abdulrahman ; Alkhairallah, Thamer ; AlSous, M Walid ; Farah, Samir ; Abu-Amero, Khaled K

BMC medical genetics, 2007-11, Vol.8 (1), p.67-67, Article 67 [Periódico revisado por pares]

England: BioMed Central Ltd

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