skip to main content
Idioma:
Resultados 1 2 3 4 next page
Mostrar Somente
Refinado por: assunto: Adult 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
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families

Bohlega, Saeed A ; Al-Mubarak, Bashayer R ; Alyemni, Eman A ; Abouelhoda, Mohamed ; Monies, Dorota ; Mustafa, Abeer E ; Khalil, Dania S ; Al Haibi, Sara ; Abou Al-Shaar, Hussam ; Faquih, Tariq ; El-Kalioby, Mohamed ; Tahir, Asma I ; Al Tassan, Nada A

BMC research notes, 2016-06, Vol.9 (1), p.295-295, Article 295 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
4
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
5
Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia

Bohlega, Saeed A ; Shinwari, Jameela M ; Al Sharif, Latifa J ; Khalil, Dania S ; Alkhairallah, Thamer S ; Al Tassan, Nada A

BMC medical genetics, 2011-02, Vol.12 (1), p.27-27, Article 27 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
6
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome

Monies, Dorota M ; Al-Hindi, Hindi N ; Al-Muhaizea, Mohamed A ; Jaroudi, Dyala J ; Al-Younes, Banan ; Naim, Ewa A ; Wakil, Salma M ; Meyer, Brian F ; Bohlega, Saeed

Neuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.353-359 [Periódico revisado por pares]

England: Elsevier B.V

Texto completo disponível

Citações Citado por
7
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
8
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
9
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
10
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis
Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis

Wakil, Salma M ; Murad, Hatem N ; Baz, Batoul M ; Hagos, Samiya T ; Al-Amr, Rana A ; Al-Yamani, Suad A ; Al-Wadaee, Salem M ; Meyer, Brian F ; Bohlega, Saeed A

Neurosciences (Riyadh, Saudi Arabia), 2012-01, Vol.17 (1), p.48-52 [Periódico revisado por pares]

Saudi Arabia

Sem texto completo

Citações Citado por
Resultados 1 2 3 4 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (21)
  2. Revistas revisadas por pares (30)

Data de Publicação 

De até
Refinar
  1. Antes de1995  (4)
  2. 1995Até1999  (9)
  3. 2000Até2003  (4)
  4. 2004Até2009  (5)
  5. Após 2009  (10)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.