skip to main content
Idioma:
Mostrar Somente
Refinado por: assunto: Genetics 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
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution
Material Type:
Artigo 		Adicionar ao Meu Espaço

Nine Hereditary Movement Disorders First Described in Asia: Their History and Evolution

Jagota, Priya ; Ugawa, Yoshikazu ; Aldaajani, Zakiyah ; Ibrahim, Norlinah Mohamed ; Ishiura, Hiroyuki ; Nomura, Yoshiko ; Tsuji, Shoji ; Diesta, Cid ; Hattori, Nobutaka ; Onodera, Osamu ; Bohlega, Saeed ; Al-Din, Amir ; Lim, Shen-Yang ; Lee, Jee-Young ; Jeon, Beomseok ; Pal, Pramod Kumar ; Shang, Huifang ; Fujioka, Shinsuke ; Kukkle, Prashanth Lingappa ; Phokaewvarangkul, Onanong ; Lin, Chin-Hsien ; Shambetova, Cholpon ; Bhidayasiri, Roongroj

Journal Of Movement Disorders, 2023, 16(3), , pp.231-247 [Periódico revisado por pares]

The Korean Movement Disorder Society

Texto completo disponível

Citações Citado por
3
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
4
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
Material Type:
Artigo 		Adicionar ao Meu Espaço

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

Texto completo disponível

Citações Citado por
5
Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features
Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features
Material Type:
Artigo 		Adicionar ao Meu Espaço

Miyoshi myopathy in Saudi Arabia: clinical, electrophysiological, histopathological and radiological features

Cupler, Edward J ; Bohlega, Saeed ; Hessler, Richard ; McLean, Donald ; Stigsby, Bent ; Ahmad, Javed

Neuromuscular disorders : NMD, 1998-06, Vol.8 (5), p.321-326 [Periódico revisado por pares]

England: Elsevier B.V

Texto completo disponível

Citações Citado por
6
Additional file 4: of Identification of a novel genetic locus underlying tremor and dystonia
Additional file 4: of Identification of a novel genetic locus underlying tremor and dystonia
Material Type:
Dataset 		Adicionar ao Meu Espaço

Additional file 4: of Identification of a novel genetic locus underlying tremor and dystonia

Monies, Dorota ; Al-Shaar, Hussam ; Goljan, Ewa ; Banan Al-Younes ; Al-Breacan, Muna ; Al-Saif, Maher ; Wakil, Salma ; Meyer, Brian ; Khabar, Khalid ; Bohlega, Saeed

Figshare 2017

Texto completo disponível

Citações Citado por
7
Additional file 3: of Identification of a novel genetic locus underlying tremor and dystonia
Additional file 3: of Identification of a novel genetic locus underlying tremor and dystonia
Material Type:
Dataset 		Adicionar ao Meu Espaço

Additional file 3: of Identification of a novel genetic locus underlying tremor and dystonia

Monies, Dorota ; Al-Shaar, Hussam ; Goljan, Ewa ; Banan Al-Younes ; Al-Breacan, Muna ; Al-Saif, Maher ; Wakil, Salma ; Meyer, Brian ; Khabar, Khalid ; Bohlega, Saeed

Figshare 2017

Texto completo disponível

Citações Citado por
8
Additional file 2: of Identification of a novel genetic locus underlying tremor and dystonia
Additional file 2: of Identification of a novel genetic locus underlying tremor and dystonia
Material Type:
Dataset 		Adicionar ao Meu Espaço

Additional file 2: of Identification of a novel genetic locus underlying tremor and dystonia

Monies, Dorota ; Al-Shaar, Hussam ; Goljan, Ewa ; Banan Al-Younes ; Al-Breacan, Muna ; Al-Saif, Maher ; Wakil, Salma ; Meyer, Brian ; Khabar, Khalid ; Bohlega, Saeed

Figshare 2017

Texto completo disponível

Citações Citado por
9
Additional file 2: of A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
Additional file 2: of A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies
Material Type:
Dataset 		Adicionar ao Meu Espaço

Additional file 2: of A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies

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

Figshare 2016

Texto completo disponível

Citações Citado por
10
The role of the PLA2G6 gene in neurodegenerative diseases
The role of the PLA2G6 gene in neurodegenerative diseases
Material Type:
Artigo 		Adicionar ao Meu Espaço

The role of the PLA2G6 gene in neurodegenerative diseases

Deng, Xinyue ; Yuan, Lamei ; Jankovic, Joseph ; Deng, Hao

Ageing research reviews, 2023-08, Vol.89, p.101957-101957, Article 101957 [Periódico revisado por pares]

England: Elsevier B.V

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Revistas revisadas por pares (8)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (8)
  2. Conjunto de Dados  (4)
  3. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1998  (1)
  2. 1998Até2010  (1)
  3. 2011Até2013  (2)
  4. 2014Até2015  (2)
  5. Após 2015  (7)
  6. Mais opções open sub menu

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

Buscando em bases de dados remotas. Favor aguardar.