Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
11 |
Material Type: Artigo
|
![]() |
Parkinson's Disease in Saudi Patients: A Genetic StudyAl-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 ScienceTexto completo disponível |
12 |
Material Type: Artigo
|
![]() |
Consensus guidelines for botulinum toxin therapy: general algorithms and dosing tables for dystonia and spasticityDressler, Dirk ; Altavista, Maria Concetta ; Altenmueller, Eckart ; Bhidayasiri, Roongroj ; Bohlega, Saeed ; Chana, Pedro ; Chung, Tae Mo ; Colosimo, Carlo ; Fheodoroff, Klemens ; Garcia-Ruiz, Pedro J. ; Jeon, Beomseok ; Jin, Lingjing ; Kanovsky, Petr ; Milanov, Ivan ; Micheli, Federico ; Orlova, Olga ; Pandey, Sanjay ; Pirtosek, Zvezdan ; Relja, Maja ; Rosales, Raymond ; Sagástegui-Rodríguez, José Alberto ; Shahidi, Gholam Ali ; Timerbaeva, Sofia ; Wan, Xinhua ; Walter, Uwe ; Saberi, Fereshte AdibJournal of Neural Transmission, 2021-03, Vol.128 (3), p.321-335 [Periódico revisado por pares]Vienna: Springer ViennaTexto completo disponível |
13 |
Material Type: Artigo
|
![]() |
Methanol-induced parkinsonism and cerebral vasculopathy due to perfume inhalationB Mohammed, Walaa ; Tarabzouni, Salma ; Bohlega, SaeedBMJ neurology open, 2022-05, Vol.4 (1), p.e000221-e000221 [Periódico revisado por pares]England: BMJ Publishing Group LtdTexto completo disponível |
14 |
Material Type: Artigo
|
![]() |
Integrated Analysis of Whole Exome Sequencing and Copy Number Evaluation in Parkinson's DiseaseYemni, 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, NadaScientific reports, 2019-03, Vol.9 (1), p.3344-3344, Article 3344 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
15 |
Material Type: Artigo
|
![]() |
Novel mutation of the notch3 gene in arabic family with CADASILBohlega, SaeedNeurology international, 2011-07, Vol.3 (2), p.e6-e6 [Periódico revisado por pares]Italy: MDPI AGTexto completo disponível |
16 |
Material Type: Artigo
|
![]() |
Clinical, Neurophysiological, Radiological, Pathological, and Genetic Features of Dysferlinopathy in Saudi ArabiaAlharbi, Norah ; Matar, Rawan ; Cupler, Edward ; Al-Hindi, Hindi ; Murad, Hatem ; Alhomud, Iftteah ; Monies, Dorota ; Alshehri, Ali ; Alyahya, Mossaed ; Meyer, Brian ; Bohlega, SaeedFrontiers in neuroscience, 2022-02, Vol.16, p.815556-815556 [Periódico revisado por pares]Switzerland: Frontiers Research FoundationTexto completo disponível |
17 |
Material Type: Artigo
|
![]() |
Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegiaWakil, Salma M ; Alhissi, Safa ; Al Dossari, Haya ; Alqahtani, Ayesha ; Shibin, Sherin ; Melaiki, Brahim T ; Finsterer, Josef ; Al-Hashem, Amal ; Bohlega, Saeed ; Alazami, Anas MBMC medical genetics, 2019-07, Vol.20 (1), p.119-119, Article 119 [Periódico revisado por pares]England: BioMed Central LtdTexto completo disponível |
18 |
Material Type: Artigo
|
![]() |
Clinical, neurophysiological, radiological, pathological, and genetic feature of Dysferlinopathy in Saudi ArabiaAlharbi, Norah ; Bohlega, Saeed ; Alhindi, Hindi ; Matar, RawanJournal of the neurological sciences, 2023-12, Vol.455, p.122521, Article 122521 [Periódico revisado por pares]Texto completo disponível |
19 |
Material Type: Artigo
|
![]() |
Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)Abusrair, Ali ; Bohlega, SaeedNeurology, 2019-04, Vol.92 (15_supplement) [Periódico revisado por pares]Texto completo disponível |
20 |
Material Type: Artigo
|
![]() |
LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutationBohlega, Saeed A ; Alfawaz, Sarah ; Abou-Al-Shaar, Hussam ; Al-Hindi, Hindi N ; Murad, Hatem N ; Bohlega, Mohamed S ; Meyer, Brian F ; Monies, DorotaActa myologica, 2018-09, Vol.37 (3), p.221-226 [Periódico revisado por pares]Italy: Pacini Editore srlTexto completo disponível |