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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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2
Primary Sjögren's syndrome with central nervous system involvement
Primary Sjögren's syndrome with central nervous system involvement
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Primary Sjögren's syndrome with central nervous system involvement

ALHOMOUD, Iftetah A ; BOHLEGA, Saeed A ; ALKAWI, Mohammed Z ; ALSEMARI, Abdulaziz M ; OMER, Saleh M ; ALSENANI, Fahmi M

Saudi medical journal, 2009-08, Vol.30 (8), p.1067-1072 [Periódico revisado por pares]

Riyadh: Saudi Medical Journal

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3
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs
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Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs

BOHLEGA, Saeed A ; ABU-AMERO, Khaled K

Saudi medical journal, 2008-07, Vol.29 (7), p.952-956 [Periódico revisado por pares]

Riyadh: Saudi Medical Journal

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4
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report
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A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Abu-Amero, Khaled K ; Al-Dhalaan, Hesham ; Bohlega, Saeed ; Hellani, Ali ; Taylor, Robert W

Journal of medical case reports, 2009-10, Vol.3 (1), p.77-77, Article 77 [Periódico revisado por pares]

England: BioMed Central Ltd

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5
Absence of mtDNA mutations in leukocytes of CADASIL patients
Absence of mtDNA mutations in leukocytes of CADASIL patients
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Absence of mtDNA mutations in leukocytes of CADASIL patients

Abu-Amero, Khaled K ; Hellani, Ali ; Bohlega, Saeed

BMC research notes, 2008-05, Vol.1 (1), p.16-16 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome
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Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome

Alazami, Anas M. ; Al-Saif, Amr ; Al-Semari, Abdulaziz ; Bohlega, Saeed ; Zlitni, Soumaya ; Alzahrani, Fatema ; Bavi, Prashant ; Kaya, Namik ; Colak, Dilek ; Khalak, Hanif ; Baltus, Andy ; Peterlin, Borut ; Danda, Sumita ; Bhatia, Kailash P. ; Schneider, Susanne A. ; Sakati, Nadia ; Walsh, Christopher A. ; Al-Mohanna, Futwan ; Meyer, Brian ; Alkuraya, Fowzan S.

American journal of human genetics, 2008-12, Vol.83 (6), p.684-691 [Periódico revisado por pares]

United States: Elsevier Inc

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7
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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8
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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9
Pan-Arab consensus statement on the use of botulinum toxin type A in spasticity management
Pan-Arab consensus statement on the use of botulinum toxin type A in spasticity management
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Pan-Arab consensus statement on the use of botulinum toxin type A in spasticity management

Aldosari, Mohammed S ; Bohlega, Saeed A ; Al-Jadid, Maher A ; El-Tamawy, Mohamed S ; Ramadan, Mohamed A ; Mousali, Yahya K ; Yaghmour, Aisha T ; Kurdi, Ashraf M ; Koussa, Salam H ; Khamis, Shaker N ; Zeljic, Vesna E ; Shacfe, Hassan D ; Molteni, Franco G

Neurosciences (Riyadh, Saudi Arabia), 2007-10, Vol.12 (4), p.279-281 [Periódico revisado por pares]

Saudi Arabia

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10
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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