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Refinado por: assunto: Male remover
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11
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

Alazami, Anas M ; Alzahrani, Fatema ; Bohlega, Saeed ; Alkuraya, Fowzan S

Neurology, 2014-05, Vol.82 (18), p.1665-1666 [Periódico revisado por pares]

United States: American Academy of Neurology

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12
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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13
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
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Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia

Alshubaili, Asmahan ; Abou-Al-Shaar, Hussam ; Santhamoorthy, Ponnusamy ; Attia, Hosam ; Bohlega, Saeed

BMC neurology, 2016-11, Vol.16 (1), p.226-226, Article 226 [Periódico revisado por pares]

England: BioMed Central Ltd

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14
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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15
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
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Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues

Bohlega, Saeed ; Al-Ajlan, Huda ; Al-Saif, Amr

European journal of human genetics : EJHG, 2014-05, Vol.22 (5), p.640-643 [Periódico revisado por pares]

England: Nature Publishing Group

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16
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families
Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families
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Accelerating Novel Candidate Gene Discovery in Neurogenetic Disorders via Whole-Exome Sequencing of Prescreened Multiplex Consanguineous Families

Alazami, Anas M. ; Patel, Nisha ; Shamseldin, Hanan E. ; Anazi, Shamsa ; Al-Dosari, Mohammed S. ; Alzahrani, Fatema ; Hijazi, Hadia ; Alshammari, Muneera ; Aldahmesh, Mohammed A. ; Salih, Mustafa A. ; Faqeih, Eissa ; Alhashem, Amal ; Bashiri, Fahad A. ; Al-Owain, Mohammed ; Kentab, Amal Y. ; Sogaty, Sameera ; Al Tala, Saeed ; Temsah, Mohamad-Hani ; Tulbah, Maha ; Aljelaify, Rasha F. ; Alshahwan, Saad A. ; Seidahmed, Mohammed Zain ; Alhadid, Adnan A. ; Aldhalaan, Hesham ; AlQallaf, Fatema ; Kurdi, Wesam ; Alfadhel, Majid ; Babay, Zainab ; Alsogheer, Mohammad ; Kaya, Namik ; Al-Hassnan, Zuhair N. ; Abdel-Salam, Ghada M.H. ; Al-Sannaa, Nouriya ; Al Mutairi, Fuad ; El Khashab, Heba Y. ; Bohlega, Saeed ; Jia, Xiaofei ; Nguyen, Henry C. ; Hammami, Rakad ; Adly, Nouran ; Mohamed, Jawahir Y. ; Abdulwahab, Firdous ; Ibrahim, Niema ; Naim, Ewa A. ; Al-Younes, Banan ; Meyer, Brian F. ; Hashem, Mais ; Shaheen, Ranad ; Xiong, Yong ; Abouelhoda, Mohamed ; Aldeeri, Abdulrahman A. ; Monies, Dorota M. ; Alkuraya, Fowzan S.

Cell reports (Cambridge), 2015-01, Vol.10 (2), p.148-161 [Periódico revisado por pares]

United States: Elsevier Inc

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17
Cyclosporine-induced migraine with severe vomiting causing loss of renal graft
Cyclosporine-induced migraine with severe vomiting causing loss of renal graft
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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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18
Clinical and genetic features of anoctaminopathy in Saudi Arabia
Clinical and genetic features of anoctaminopathy in Saudi Arabia
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Clinical and genetic features of anoctaminopathy in Saudi Arabia

Bohlega, Saeed ; Monies, Dorothy M ; Abulaban, Ahmad A ; Murad, Hatem N ; Alhindi, Hindi N ; Meyer, Brian F

Neurosciences (Riyadh, Saudi Arabia), 2015-04, Vol.20 (2), p.173-177 [Periódico revisado por pares]

Saudi Arabia: Riyadh : Armed Forces Hospital

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19
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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20
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula
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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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