skip to main content
Idioma:
Mostrar Somente
Refinado por: assunto: Middle Aged remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Parkinson's Disease in Saudi Patients: A Genetic Study
Parkinson's Disease in Saudi Patients: A Genetic Study
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
2
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation
Material Type:
Artigo 		Adicionar ao Meu Espaço

LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation

Bohlega, Saeed A ; Alfawaz, Sarah ; Abou-Al-Shaar, Hussam ; Al-Hindi, Hindi N ; Murad, Hatem N ; Bohlega, Mohamed S ; Meyer, Brian F ; Monies, Dorota

Acta myologica, 2018-09, Vol.37 (3), p.221-226 [Periódico revisado por pares]

Italy: Pacini Editore srl

Texto completo disponível

Citações Citado por
3
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
4
CADASIL in Arabs: clinical and genetic findings
CADASIL in Arabs: clinical and genetic findings
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
5
Primary Sjögren's syndrome with central nervous system involvement
Primary Sjögren's syndrome with central nervous system involvement
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Sem texto completo

Citações Citado por
6
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Sem texto completo

Citações Citado por
7
The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia
The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia
Material Type:
Artigo 		Adicionar ao Meu Espaço

The expansion of the CAG repeat in ataxin-2 is a frequent cause of autosomal dominant spinocerebellar ataxia

LORENZETTI, D ; BOHLEGA, S ; ZOGHBI, H. Y

Neurology, 1997-10, Vol.49 (4), p.1009-1013 [Periódico revisado por pares]

Hagerstown, MD: Lippincott Williams & Wilkins

Sem texto completo

Citações Citado por
8
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
9
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
10
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (14)

Data de Publicação 

De até
Refinar
  1. Antes de1997  (2)
  2. 1997Até2000  (4)
  3. 2001Até2003  (2)
  4. 2004Até2008  (3)
  5. Após 2008  (8)
  6. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.