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1
Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know
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Cladribine Tablets and Relapsing–Remitting Multiple Sclerosis: A Pragmatic, Narrative Review of What Physicians Need to Know

AlJumah, Mohamed ; Alkhawajah, Mona Marwan ; Qureshi, Shireen ; Al-Thubaiti, Ibtisam ; Ayoub, Omar ; Bohlega, Saeed A. ; Bushnag, Areej ; Cupler, Edward ; Daif, Abdulkader ; El Boghdady, Ahmed ; Hassan, Ahmed ; Al Malik, Yaser ; Saeedi, Jameelah ; Al-Shamrany, Fawzia ; Shosha, Eslam ; Rieckmann, Peter

Neurology and therapy, 2020-06, Vol.9 (1), p.11-23 [Periódico revisado por pares]

Cheshire: Springer Healthcare

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2
Parkinson's Disease in Saudi Patients: A Genetic Study
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Artigo
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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

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3
Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review
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Artigo
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Immune Reconstitution Therapy or Continuous Immunosuppression for the Management of Active Relapsing–Remitting Multiple Sclerosis Patients? A Narrative Review

AlSharoqi, Isa Ahmed ; Aljumah, Mohamed ; Bohlega, Saeed ; Boz, Cavit ; Daif, Abdelkader ; El-Koussa, Salam ; Inshasi, Jihad ; Kurtuncu, Murat ; Müller, Thomas ; Retief, Chris ; Sahraian, Mohammad Ali ; Shaygannejad, Vahid ; Slassi, Ilham ; Taha, Karim ; Zakaria, Magd ; Sørensen, Per Soelberg

Neurology and therapy, 2020-06, Vol.9 (1), p.55-66 [Periódico revisado por pares]

Cheshire: Springer Healthcare

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4
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
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Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy

Brown, Robert H ; Liu, Jing ; Aoki, Masashi ; Illa, Isabel ; Wu, Chenyan ; Fardeau, Michel ; Angelini, Corrado ; Serrano, Carmen ; Urtizberea, J. Andoni ; Hentati, Faycal ; Hamida, Mongi Ben ; Bohlega, Saeed ; Culper, Edward J ; Amato, Anthony A ; Bossie, Karen ; Oeltjen, Joshua ; Bejaoui, Khemissa ; McKenna-Yasek, Diane ; Hosler, Betsy A ; Schurr, Erwin ; Arahata, Kiichi ; de Jong, Pieter J

Nature genetics, 1998-09, Vol.20 (1), p.31-36 [Periódico revisado por pares]

London: Nature Publishing Group

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5
Mutations in NHLRC1 cause progressive myoclonus epilepsy
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Mutations in NHLRC1 cause progressive myoclonus epilepsy

Minassian, Berge A ; Scherer, Stephen W ; Chan, Elayne M ; Young, Edwin J ; Ianzano, Leonarda ; Munteanu, Iulia ; Zhao, Xiaochu ; Christopoulos, Constantine C ; Avanzini, Giuliano ; Elia, Maurizio ; Ackerley, Cameron A ; Jovic, Nebojsa J ; Bohlega, Saeed ; Andermann, Eva ; Rouleau, Guy A ; Delgado-Escueta, Antonio V

Nature genetics, 2003-10, Vol.35 (2), p.125-127 [Periódico revisado por pares]

London: Nature Publishing Group

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6
Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegia
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Multiphasic disseminated encephalomyelitis presenting as alternating hemiplegia

Khan, S ; Yaqub, B A ; Poser, C M ; al Deeb, S M ; Bohlega, S

Journal of neurology, neurosurgery and psychiatry, 1995-04, Vol.58 (4), p.467-470 [Periódico revisado por pares]

London: BMJ Publishing Group Ltd

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7
A novel variant of PLA2G6 gene related early-onset parkinsonism: a case report and literature review
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Artigo
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A novel variant of PLA2G6 gene related early-onset parkinsonism: a case report and literature review

Cai, Dapeng ; Wu, Haohao ; Huang, Baogang ; Xiao, Weiwei ; Du, Kang

Frontiers in neurology, 2024-04, Vol.15, p.1349861 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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8
Genotype-Phenotype Correlations in Monogenic Parkinson Disease: A Review on Clinical and Molecular Findings
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Genotype-Phenotype Correlations in Monogenic Parkinson Disease: A Review on Clinical and Molecular Findings

Guadagnolo, Daniele ; Piane, Maria ; Torrisi, Maria Rosaria ; Pizzuti, Antonio ; Petrucci, Simona

Frontiers in neurology, 2021-09, Vol.12, p.648588-648588 [Periódico revisado por pares]

Frontiers Media S.A

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9
Early-Onset Parkinson's Disease Caused by PLA2G6 Compound Heterozygous Mutation, a Case Report and Literature Review
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Artigo
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Early-Onset Parkinson's Disease Caused by PLA2G6 Compound Heterozygous Mutation, a Case Report and Literature Review

Shen, Ting ; Hu, Jing ; Jiang, Yasi ; Zhao, Shuai ; Lin, Caixiu ; Yin, Xinzhen ; Yan, Yaping ; Pu, Jiali ; Lai, Hsin-Yi ; Zhang, Baorong

Frontiers in neurology, 2019-08, Vol.10, p.915 [Periódico revisado por pares]

Switzerland: Frontiers Research Foundation

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10
Novel PLA2G6 Pathogenic Variants in Chinese Patients With PLA2G6-Associated Neurodegeneration
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Novel PLA2G6 Pathogenic Variants in Chinese Patients With PLA2G6-Associated Neurodegeneration

Wan, Yalan ; Jiang, Yanyan ; Xie, Zhiying ; Ling, Chen ; Du, Kang ; Li, Ran ; Yuan, Yun ; Wang, Zhaoxia ; Sun, Wei ; Jin, Haiqiang

Frontiers in neurology, 2022-07, Vol.13, p.922528-922528 [Periódico revisado por pares]

Frontiers Media S.A

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