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Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)
Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)
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Hypogonadism, alopecia and neurological manifestations: evolving syndromes from an old association. (P4.9-060)

Abusrair, Ali ; Bohlega, Saeed

Neurology, 2019-04, Vol.92 (15_supplement) [Periódico revisado por pares]

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2
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)
Expanding the genotype-phenotype landscape of PDE10A-associated movement disorders (S42.004)
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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, Stefan

Neurology, 2023-04, Vol.100 (17_supplement_2) [Periódico revisado por pares]

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3
Brain MRI findings in Woodhouse-Sakati Syndrome (P6.071)
Brain MRI findings in Woodhouse-Sakati Syndrome (P6.071)
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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, Amaal

Neurology, 2018-04, Vol.90 (15_supplement) [Periódico revisado por pares]

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4
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3
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SET binding factor 1 (SBF1) mutation causes Charcot-Marie-Tooth disease type 4B3

Alazami, Anas M ; Alzahrani, Fatema ; Bohlega, Saeed ; Alkuraya, Fowzan S

Neurology, 2014-05, Vol.82 (18), p.1665-1666 [Periódico revisado por pares]

United States: American Academy of Neurology

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5
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)
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)
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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, Edward

Neurology, 2017-04, Vol.88 (16_supplement) [Periódico revisado por pares]

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6
Homozygous Non-Sense Mutation in Atlastin-1 Gene Caused Pure Hereditary Spastic Paraplegia (P2.236)
Homozygous Non-Sense Mutation in Atlastin-1 Gene Caused Pure Hereditary Spastic Paraplegia (P2.236)
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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, Salma

Neurology, 2015-04, Vol.84 (14_supplement) [Periódico revisado por pares]

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7
Levodopa/Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson Disease - The Saudi Arabian Experience (P3.024)
Levodopa/Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson Disease - The Saudi Arabian Experience (P3.024)
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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, Khalid

Neurology, 2015-04, Vol.84 (14_supplement) [Periódico revisado por pares]

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8
Complicated Hereditary Paraplegia with Novel B4GALNT1 Mutations Expanding, the Phenotype and Genotype (P7.075)
Complicated Hereditary Paraplegia with Novel B4GALNT1 Mutations Expanding, the Phenotype and Genotype (P7.075)
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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, Brian

Neurology, 2014-04, Vol.82 (10_supplement) [Periódico revisado por pares]

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9
Teaching neuroimages: harlequin syndrome caused by lesion of sympathetic regulatory neurons
Teaching neuroimages: harlequin syndrome caused by lesion of sympathetic regulatory neurons
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Teaching neuroimages: harlequin syndrome caused by lesion of sympathetic regulatory neurons

Bohlega, Saeed ; Stigsby, Bent ; Al Mohaileb, Fahd

Neurology, 2010-06, Vol.74 (24), p.e106-e106 [Periódico revisado por pares]

United States

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10
Teaching Neuro Images : Harlequin syndrome caused by lesion of sympathetic regulatory neurons
Teaching Neuro Images : Harlequin syndrome caused by lesion of sympathetic regulatory neurons
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Teaching Neuro Images : Harlequin syndrome caused by lesion of sympathetic regulatory neurons

Bohlega, Saeed ; Stigsby, Bent ; Al Mohaileb, Fahd

Neurology, 2010-06, Vol.74 (24) [Periódico revisado por pares]

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