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1 |
Material Type: Artículo
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Mutations in the J domain of DNAJB6 cause dominant distal myopathyPalmio, Johanna ; Jonson, Per Harald ; Inoue, Michio ; Sarparanta, Jaakko ; Bengoechea, Rocio ; Savarese, Marco ; Vihola, Anna ; Jokela, Manu ; Nakagawa, Masanori ; Noguchi, Satoru ; Olivé, Montse ; Masingue, Marion ; Kerty, Emilia ; Hackman, Peter ; Weihl, Conrad C. ; Nishino, Ichizo ; Udd, BjarneNeuromuscular disorders : NMD, 2020-01, Vol.30 (1), p.38-46 [Revista revisada por pares]England: Elsevier B.VTexto completo disponible |
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2 |
Material Type: Artículo
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Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese familiesLi, Shan ; You, Yi ; Gao, Jinsong ; Mao, Bin ; Cao, Yixuan ; Zhao, Xiuli ; Zhang, XueBMC medical genetics, 2018-10, Vol.19 (1), p.179-179, Article 179 [Revista revisada por pares]England: BioMed Central LtdTexto completo disponible |
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3 |
Material Type: Artículo
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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 [Revista revisada por pares]Pacini Editore srlTexto completo disponible |
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4 |
Material Type: Artículo
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Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesiaAlshubaili, Asmahan ; Abou-Al-Shaar, Hussam ; Santhamoorthy, Ponnusamy ; Attia, Hosam ; Bohlega, SaeedBMC neurology, 2016-11, Vol.16 (1), p.226-226, Article 226 [Revista revisada por pares]England: BioMed Central LtdTexto completo disponible |
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5 |
Material Type: Artículo
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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL familyAl-Shaar, Hussam Abou ; Qadi, Najeeb ; Ahmed, Mohammed ; Meyer, Brian F ; Bohlega, SaeedJournal of the neurological sciences, 2016-08, Vol.367, p.239-243 [Revista revisada por pares]Netherlands: Elsevier B.VTexto completo disponible |
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6 |
Material Type: Artículo
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Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi familiesBohlega, 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 ABMC research notes, 2016-06, Vol.9 (1), p.295-295, Article 295 [Revista revisada por pares]England: BioMed Central LtdTexto completo disponible |
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7 |
Material Type: Artículo
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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 [Revista revisada por pares]United States: Public Library of ScienceTexto completo disponible |
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8 |
Material Type: Artículo
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Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center ExperienceBohlega, Saeed ; Abou Al-Shaar, Hussam ; Alkhairallah, Thamer ; Al-Ajlan, Fahad ; Hasan, Nael ; Alkahtani, KhalidEuropean neurology, 2015-01, Vol.74 (5-6), p.227-236 [Revista revisada por pares]Basel, Switzerland: S. Karger AGTexto completo disponible |
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9 |
Material Type: Artículo
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Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndromeMonies, 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, SaeedNeuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.353-359 [Revista revisada por pares]England: Elsevier B.VTexto completo disponible |
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10 |
Material Type: Artículo
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A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxiaAl Tassan, Nada ; Khalil, Dania ; Shinwari, Jameela ; Al Sharif, Latifa ; Bavi, Prashant ; Abduljaleel, Zainularifeen ; Abu Dhaim, Nada ; Magrashi, Amna ; Bobis, Steve ; Ahmed, Hala ; AlAhmed, Samaher ; Bohlega, SaeedHuman mutation, 2012-02, Vol.33 (2), p.351-354 [Revista revisada por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponible |