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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, Vol.74(24), pp.e106-e106 [Periódico revisado por pares]

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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family
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Phenotypic comparison of individuals with homozygous or heterozygous mutation of NOTCH3 in a large CADASIL family

Abou Al-Shaar, Hussam ; Qadi, Najeeb ; Al-Hamed, Mohamed H ; Meyer, Brian F ; Bohlega, Saeed

Journal of the Neurological Sciences, 15 August 2016, Vol.367, pp.239-243 [Periódico revisado por pares]

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3
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues
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Mutation of fibulin-1 causes a novel syndrome involving the central nervous system and connective tissues

Saeed Bohlega ; Huda Al-Ajlan ; Amr Al-Saif

European Journal of Human Genetics, 2013, Vol.22(5), p.640 [Periódico revisado por pares]

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4
Parkinson's Disease in Saudi Patients: A Genetic Study
Parkinson's Disease in Saudi Patients: A Genetic Study
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Parkinson's Disease in Saudi Patients: A Genetic Study

Bashayer R Al-Mubarak ; Saeed A Bohlega ; Thamer S Alkhairallah ; Amna I Magrashi ; Maha I Alturki ; Dania S Khalil ; Basma S Alabdulaziz ; Hussam Abou Al-Shaar ; Abeer E Mustafa ; Eman A Alyemni ; Bashayer A Alsaffar ; Asma I Tahir ; Nada A Al Tassan

PLoS ONE, 01 January 2015, Vol.10(8), p.e0135950 [Periódico revisado por pares]

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5
Neurological complications in liver transplantation
Neurological complications in liver transplantation
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Neurological complications in liver transplantation

Ghaus, Naveed ; Bohlega, Saeed ; Rezeig, Mohammed

Journal of Neurology, 2001, Vol.248(12), pp.1042-1048 [Periódico revisado por pares]

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6
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia
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Ultrasound-guided botulinum toxin A injection in the treatment of belly dancer's dyskinesia

Alshubaili, Asmahan ; Abou-Al-Shaar, Hussam ; Santhamoorthy, Ponnusamy ; Attia, Hosam ; Bohlega, Saeed

BMC neurology, 17 November 2016, Vol.16(1), pp.226 [Periódico revisado por pares]

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7
MRI findings in neuro-Behcetʼs disease
MRI findings in neuro-Behcetʼs disease
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MRI findings in neuro-Behcetʼs disease

Al Kawi, Zuheir, M. ; Bohlega, Zuheir, Saeed ; Banna, Zuheir, Mohamed

Neurology, 1991, Vol.41(3), pp.405-408 [Periódico revisado por pares]

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8
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T
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Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C>T

Wakil, Salma M ; Ramzan, Khushnooda ; Abuthuraya, Rula ; Hagos, Samya ; Al-Dossari, Haya ; Al-Omar, Rana ; Murad, Hatem ; Chedrawi, Aziza ; Al-Hassnan, Zuhair N ; Finsterer, Josef ; Bohlega, Saeed

Gene, 15 February 2014, Vol.536(1), pp.217-220 [Periódico revisado por pares]

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9
Identification of a novel genetic locus underlying tremor and dystonia.(Report)
Identification of a novel genetic locus underlying tremor and dystonia.(Report)
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Identification of a novel genetic locus underlying tremor and dystonia.(Report)

Monies, Dorota ; Al-Shaar, Hussam Abou ; Goljan, Ewa A. ; Al-Younes, Banan ; Al-Breacan, Muna Monther Abdullah ; Al-Saif, Maher Mohammed ; Wakil, Salma M. ; Meyer, Brian F. ; Khabar, Khalid S. A. ; Bohlega, Saeed

Human Genomics, Nov 6, 2017, Vol.11(1) [Periódico revisado por pares]

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10
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome
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Clinical and pathological heterogeneity of a congenital disorder of glycosylation manifesting as a myasthenic/myopathic syndrome

Monies, 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, Saeed

Neuromuscular Disorders, April 2014, Vol.24(4), pp.353-359 [Periódico revisado por pares]

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Deste Autor:

  1. Bohlega, Saeed
  2. Bohlega, S.
  3. Meyer, Brian F
  4. Bohlega, Saeed A
  5. Abou Al-Shaar, Hussam

Neste Assunto:

  1. Humans
  2. Male
  3. Medicine
  4. Adult
  5. Mutation

  • Realização: USP

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