skip to main content
Idioma:
Primo Advanced Search
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search prefilters
Busca Simples
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: Base de dados/Biblioteca: IngentaConnect Journals remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine
Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine
Material Type:
Artigo 		Adicionar ao Meu Espaço

Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine

Marashly, Eyad T ; Bohlega, Saeed A

Frontiers in neurology, 2017-07, Vol.8, p.333-333 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

Texto completo disponível

Citações Citado por
2
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
3
Novel mutation of the notch3 gene in arabic family with CADASIL
Novel mutation of the notch3 gene in arabic family with CADASIL
Material Type:
Artigo 		Adicionar ao Meu Espaço

Novel mutation of the notch3 gene in arabic family with CADASIL

Bohlega, Saeed

Neurology international, 2011-07, Vol.3 (2), p.e6-e6 [Periódico revisado por pares]

Italy: MDPI AG

Texto completo disponível

Citações Citado por
4
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease
Material Type:
Artigo 		Adicionar ao Meu Espaço

Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's Disease

Yemni, Eman Al ; Monies, Dorota ; Alkhairallah, Thamer ; Bohlega, Saeed ; Abouelhoda, Mohamed ; Magrashi, Amna ; Mustafa, Abeer ; AlAbdulaziz, Basma ; Alhamed, Mohamed ; Baz, Batoul ; Goljan, Ewa ; Albar, Renad ; Jabaan, Amjad ; Faquih, Tariq ; Subhani, Shazia ; Ali, Wafa ; Shinwari, Jameela ; Al-Mubarak, Bashayer ; Al-Tassan, Nada

Scientific reports, 2019-03, Vol.9 (1), p.3344-3344, Article 3344 [Periódico revisado por pares]

England: Nature Publishing Group

Texto completo disponível

Citações Citado por
5
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
Material Type:
Artigo 		Adicionar ao Meu Espaço

Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia

Wakil, Salma M ; Alhissi, Safa ; Al Dossari, Haya ; Alqahtani, Ayesha ; Shibin, Sherin ; Melaiki, Brahim T ; Finsterer, Josef ; Al-Hashem, Amal ; Bohlega, Saeed ; Alazami, Anas M

BMC medical genetics, 2019-07, Vol.20 (1), p.119-119, Article 119 [Periódico revisado por pares]

England: BioMed Central Ltd

Texto completo disponível

Citações Citado por
6
Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)
Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)

Abusrair, Ali ; Bohlega, Saeed

Neurology, 2019-04, Vol.92 (15_supplement) [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
7
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
8
Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome
Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome
Material Type:
Artigo 		Adicionar ao Meu Espaço

Multimodal Evoked Potential Profiles in Woodhouse-Sakati Syndrome

Abusrair, Ali ; AlHamoud, Iftetah ; Bohlega, Saeed

Journal of clinical neurophysiology, 2022-09, Vol.Publish Ahead of Print (6), p.504-509 [Periódico revisado por pares]

United States

Texto completo disponível

Citações Citado por
9
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
Material Type:
Artigo 		Adicionar ao Meu Espaço

A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies

Monies, Dorota ; Alhindi, Hindi N ; Almuhaizea, Mohamed A ; Abouelhoda, Mohamed ; Alazami, Anas M ; Goljan, Ewa ; Alyounes, Banan ; Jaroudi, Dyala ; AlIssa, Abdulelah ; Alabdulrahman, Khalid ; Subhani, Shazia ; El-Kalioby, Mohamed ; Faquih, Tariq ; Wakil, Salma M ; Altassan, Nada A ; Meyer, Brian F ; Bohlega, Saeed

Human genomics, 2016-09, Vol.10 (1), p.32-32, Article 32 [Periódico revisado por pares]

England: BioMed Central

Texto completo disponível

Citações Citado por
10
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)
Material Type:
Artigo 		Adicionar ao Meu Espaço

Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)

Bohlega, Saeed ; Al-Qahtani, Zainah ; Guzmán-Vega, Francisco J. ; Ramakrishnan, Reshmi ; Abusrair, Ali ; Aldosari, Haya ; AlDakheel, Amaal ; Al-Qahtani, Salma ; Monies, Dorota ; Arold, Stefan

Neurology, 2023-04, Vol.100 (17_supplement_2) [Periódico revisado por pares]

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (44)

Data de Publicação 

De até
Refinar
  1. Antes de2007  (4)
  2. 2007Até2012  (8)
  3. 2013Até2016  (16)
  4. 2017Até2021  (12)
  5. Após 2021  (7)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.