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Material Type: Artigo
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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 |
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Material Type: Artigo
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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, StefanNeurology, 2023-04, Vol.100 (17_supplement_2) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Brain MRI findings in Woodhouse-Sakati Syndrome (P6.071)Abusrair, Ali ; Bohlega, Saeed ; Al-Ajlan, Fahad ; Al-Semari, Abdulaziz ; Mohamed, Bader ; AlDakheel, AmaalNeurology, 2018-04, Vol.90 (15_supplement) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3Alazami, Anas M ; Alzahrani, Fatema ; Bohlega, Saeed ; Alkuraya, Fowzan SNeurology, 2014-05, Vol.82 (18), p.1665-1666 [Periódico revisado por pares]United States: American Academy of NeurologyTexto completo disponível |
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Material Type: Artigo
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Pattern reversal visual evoked potentials (prVEPs) in autosomal recessive hereditary spastic paraplegia with thin corpus callosum (ARHSPTCC) patients with SPG 11 mutations in Saudi Arabia (P2.206)Al-Faidi, Nouf ; Ali, Qurban ; Al Said, Youssef ; Karim, Gulzar ; Khan, Haji ; Bohlega, Saeed ; Cupler, EdwardNeurology, 2017-04, Vol.88 (16_supplement) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Homozygous Non-Sense Mutation in Atlastin-1 Gene Caused Pure Hereditary Spastic Paraplegia (P2.236)Saeed, Bohlega ; Abulaban, Ahmad ; Hagos, Samya ; Qahtani, Aisha ; Wakil, SalmaNeurology, 2015-04, Vol.84 (14_supplement) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Levodopa/Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson Disease - The Saudi Arabian Experience (P3.024)Saeed, Bohlega ; Alkhairallah, Thamer ; Alajlan, Fahad ; Abou Al-Shaar, Hussam ; Hasan, Nael ; Alkahtani, KhalidNeurology, 2015-04, Vol.84 (14_supplement) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Complicated Hereditary Paraplegia with Novel B4GALNT1 Mutations Expanding, the Phenotype and Genotype (P7.075)Bohlega, Saeed ; Wakil, Salma ; Monies, Dorota ; Cupler, Edward ; Bastaki, Layla ; Meyer, BrianNeurology, 2014-04, Vol.82 (10_supplement) [Periódico revisado por pares]Texto completo disponível |
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Material Type: Artigo
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Teaching neuroimages: harlequin syndrome caused by lesion of sympathetic regulatory neuronsBohlega, Saeed ; Stigsby, Bent ; Al Mohaileb, FahdNeurology, 2010-06, Vol.74 (24), p.e106-e106 [Periódico revisado por pares]United StatesTexto completo disponível |
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10 |
Material Type: Artigo
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Teaching Neuro Images : Harlequin syndrome caused by lesion of sympathetic regulatory neuronsBohlega, Saeed ; Stigsby, Bent ; Al Mohaileb, FahdNeurology, 2010-06, Vol.74 (24) [Periódico revisado por pares]Texto completo disponível |