Publications by authors named "Saeed Bohlega"

71Publications

Patterns of neurological manifestations in Woodhouse-Sakati Syndrome.

Parkinsonism Relat Disord 2019 12 13;69:99-103. Epub 2019 Oct 13.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.parkreldis.2019.10.007DOI Listing
December 2019

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Authors:
Dorota Monies Mohammed Abouelhoda Mirna Assoum Nabil Moghrabi Rafiullah Rafiullah Naif Almontashiri Mohammed Alowain Hamad Alzaidan Moeen Alsayed Shazia Subhani Edward Cupler Maha Faden Amal Alhashem Alya Qari Aziza Chedrawi Hisham Aldhalaan Wesam Kurdi Sameena Khan Zuhair Rahbeeni Maha Alotaibi Ewa Goljan Hadeel Elbardisy Mohamed ElKalioby Zeeshan Shah Hibah Alruwaili Amal Jaafar Ranad Albar Asma Akilan Hamsa Tayeb Asma Tahir Mohammed Fawzy Mohammed Nasr Shaza Makki Abdullah Alfaifi Hanna Akleh Suad Yamani Dalal Bubshait Mohammed Mahnashi Talal Basha Afaf Alsagheir Musad Abu Khaled Khalid Alsaleem Maisoon Almugbel Manal Badawi Fahad Bashiri Saeed Bohlega Raashida Sulaiman Ehab Tous Syed Ahmed Talal Algoufi Hamoud Al-Mousa Emadia Alaki Susan Alhumaidi Hadeel Alghamdi Malak Alghamdi Ahmed Sahly Shapar Nahrir Ali Al-Ahmari Hisham Alkuraya Ali Almehaidib Mohammed Abanemai Fahad Alsohaibaini Bandar Alsaud Rand Arnaout Ghada M H Abdel-Salam Hasan Aldhekri Suzan AlKhater Khalid Alqadi Essam Alsabban Turki Alshareef Khalid Awartani Hanaa Banjar Nada Alsahan Ibraheem Abosoudah Abdullah Alashwal Wajeeh Aldekhail Sami Alhajjar Sulaiman Al-Mayouf Abdulaziz Alsemari Walaa Alshuaibi Saeed Altala Abdulhadi Altalhi Salah Baz Muddathir Hamad Tariq Abalkhail Badi Alenazi Alya Alkaff Fahad Almohareb Fuad Al Mutairi Mona Alsaleh Abdullah Alsonbul Somaya Alzelaye Shakir Bahzad Abdulaziz Bin Manee Ola Jarrad Neama Meriki Bassem Albeirouti Amal Alqasmi Mohammed AlBalwi Nawal Makhseed Saeed Hassan Isam Salih Mustafa A Salih Marwan Shaheen Saadeh Sermin Shamsad Shahrukh Shahrukh Hashmi Ayman Shawli Ameen Tajuddin Abdullah Tamim Ahmed Alnahari Ibrahim Ghemlas Maged Hussein Sami Wali Hatem Murad Brian F Meyer Fowzan S Alkuraya

Am J Hum Genet 2019 Oct;105(4):879

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http://dx.doi.org/10.1016/j.ajhg.2019.09.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817532PMC
October 2019

Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia.

BMC Med Genet 2019 07 4;20(1):119. Epub 2019 Jul 4.

Department of Genetics, Research Centre, King Faisal Specialist Hospital & Research Centre, MBC-03, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.

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http://dx.doi.org/10.1186/s12881-019-0851-6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6610916PMC
July 2019

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.

Authors:
Dorota Monies Mohammed Abouelhoda Mirna Assoum Nabil Moghrabi Rafiullah Rafiullah Naif Almontashiri Mohammed Alowain Hamad Alzaidan Moeen Alsayed Shazia Subhani Edward Cupler Maha Faden Amal Alhashem Alya Qari Aziza Chedrawi Hisham Aldhalaan Wesam Kurdi Sameena Khan Zuhair Rahbeeni Maha Alotaibi Ewa Goljan Hadeel Elbardisy Mohamed ElKalioby Zeeshan Shah Hibah Alruwaili Amal Jaafar Ranad Albar Asma Akilan Hamsa Tayeb Asma Tahir Mohammed Fawzy Mohammed Nasr Shaza Makki Abdullah Alfaifi Hanna Akleh Suad Yamani Dalal Bubshait Mohammed Mahnashi Talal Basha Afaf Alsagheir Musad Abu Khaled Khalid Alsaleem Maisoon Almugbel Manal Badawi Fahad Bashiri Saeed Bohlega Raashida Sulaiman Ehab Tous Syed Ahmed Talal Algoufi Hamoud Al-Mousa Emadia Alaki Susan Alhumaidi Hadeel Alghamdi Malak Alghamdi Ahmed Sahly Shapar Nahrir Ali Al-Ahmari Hisham Alkuraya Ali Almehaidib Mohammed Abanemai Fahad Alsohaibaini Bandar Alsaud Rand Arnaout Ghada M H Abdel-Salam Hasan Aldhekri Suzan AlKhater Khalid Alqadi Essam Alsabban Turki Alshareef Khalid Awartani Hanaa Banjar Nada Alsahan Ibraheem Abosoudah Abdullah Alashwal Wajeeh Aldekhail Sami Alhajjar Sulaiman Al-Mayouf Abdulaziz Alsemari Walaa Alshuaibi Saeed Altala Abdulhadi Altalhi Salah Baz Muddathir Hamad Tariq Abalkhail Badi Alenazi Alya Alkaff Fahad Almohareb Fuad Al Mutairi Mona Alsaleh Abdullah Alsonbul Somaya Alzelaye Shakir Bahzad Abdulaziz Bin Manee Ola Jarrad Neama Meriki Bassem Albeirouti Amal Alqasmi Mohammed AlBalwi Nawal Makhseed Saeed Hassan Isam Salih Mustafa A Salih Marwan Shaheen Saadeh Sermin Shamsad Shahrukh Shahrukh Hashmi Ayman Shawli Ameen Tajuddin Abdullah Tamim Ahmed Alnahari Ibrahim Ghemlas Maged Hussein Sami Wali Hatem Murad Brian F Meyer Fowzan S Alkuraya

Am J Hum Genet 2019 06 23;104(6):1182-1201. Epub 2019 May 23.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh 12354, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2019.04.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6562004PMC
June 2019

Autosomal recessive ADCY5-Related dystonia and myoclonus: Expanding the genetic spectrum of ADCY5-Related movement disorders.

Parkinsonism Relat Disord 2019 07 28;64:145-149. Epub 2019 Feb 28.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; Department of Biomedical Research, King Fahad Specialist Hospital, Dammam, Saudi Arabia.

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http://dx.doi.org/10.1016/j.parkreldis.2019.02.039DOI Listing
July 2019

LGMD1D myopathy with cytoplasmic and nuclear inclusions in a Saudi family due to DNAJB6 mutation.

Acta Myol 2018 Sep 1;37(3):221-226. Epub 2018 Sep 1.

Department of Genetics, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390114PMC
September 2018

Riboflavin Has Neuroprotective Potential: Focus on Parkinson's Disease and Migraine.

Front Neurol 2017 20;8:333. Epub 2017 Jul 20.

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.3389/fneur.2017.00333DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5517396PMC
July 2017

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.

Authors:
Dorota Monies Mohamed Abouelhoda Moeenaldeen AlSayed Zuhair Alhassnan Maha Alotaibi Husam Kayyali Mohammed Al-Owain Ayaz Shah Zuhair Rahbeeni Mohammad A Al-Muhaizea Hamad I Alzaidan Edward Cupler Saeed Bohlega Eissa Faqeih Maha Faden Banan Alyounes Dyala Jaroudi Ewa Goljan Hadeel Elbardisy Asma Akilan Renad Albar Hesham Aldhalaan Shamshad Gulab Aziza Chedrawi Bandar K Al Saud Wesam Kurdi Nawal Makhseed Tahani Alqasim Heba Y El Khashab Hamoud Al-Mousa Amal Alhashem Imaduddin Kanaan Talal Algoufi Khalid Alsaleem Talal A Basha Fathiya Al-Murshedi Sameena Khan Adila Al-Kindy Maha Alnemer Sami Al-Hajjar Suad Alyamani Hasan Aldhekri Ali Al-Mehaidib Rand Arnaout Omar Dabbagh Mohammad Shagrani Dieter Broering Maha Tulbah Amal Alqassmi Maisoon Almugbel Mohammed AlQuaiz Abdulaziz Alsaman Khalid Al-Thihli Raashda A Sulaiman Wajeeh Al-Dekhail Abeer Alsaegh Fahad A Bashiri Alya Qari Suzan Alhomadi Hisham Alkuraya Mohammed Alsebayel Muddathir H Hamad Laszlo Szonyi Faisal Abaalkhail Sulaiman M Al-Mayouf Hamad Almojalli Khalid S Alqadi Hussien Elsiesy Taghreed M Shuaib Mohammed Zain Seidahmed Ibraheem Abosoudah Hana Akleh Abdulaziz AlGhonaium Turki M Alkharfy Fuad Al Mutairi Wafa Eyaid Abdullah Alshanbary Farrukh R Sheikh Fahad I Alsohaibani Abdullah Alsonbul Saeed Al Tala Soher Balkhy Randa Bassiouni Ahmed S Alenizi Maged H Hussein Saeed Hassan Mohamed Khalil Brahim Tabarki Saad Alshahwan Amira Oshi Yasser Sabr Saad Alsaadoun Mustafa A Salih Sarar Mohamed Habiba Sultana Abdullah Tamim Moayad El-Haj Saif Alshahrani Dalal K Bubshait Majid Alfadhel Tariq Faquih Mohamed El-Kalioby Shazia Subhani Zeeshan Shah Nabil Moghrabi Brian F Meyer Fowzan S Alkuraya

Hum Genet 2017 08 9;136(8):921-939. Epub 2017 Jun 9.

Deparment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1007/s00439-017-1821-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502059PMC
August 2017

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

BMC Neurol 2016 Nov 17;16(1):226. Epub 2016 Nov 17.

Movement Disorder Program, Division of Neurology, Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1186/s12883-016-0746-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114732PMC
November 2016

Ataxia and Hypogonadotropic Hypogonadism with Intrafamilial Variability Caused by RNF216 Mutation.

Neurol Int 2016 Jun 15;8(2):6444. Epub 2016 Jun 15.

Department of Neurosciences, King Faisal Specialist Hospital and Research Center Riyadh , Saudi Arabia.

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http://dx.doi.org/10.4081/ni.2016.6444DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4935815PMC
June 2016

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

J Neurol Sci 2016 Aug 1;367:239-43. Epub 2016 Jun 1.

Division of Neurology, Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.jns.2016.05.061DOI Listing
August 2016

Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families.

BMC Res Notes 2016 Jun 7;9:295. Epub 2016 Jun 7.

Behavioral Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, P.O Box 3354, Riyadh, 11211, Saudi Arabia.

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http://dx.doi.org/10.1186/s13104-016-2102-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897907PMC
June 2016

Woodhouse-Sakati Syndrome: Report of the First Tunisian Family with the C2orf37 Gene Mutation.

J Mov Disord 2016 May 25;9(2):120-3. Epub 2016 May 25.

Department of Neurology, Habib Bourguiba Hospital, Sfax, Tunisia.

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http://dx.doi.org/10.14802/jmd.16003DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4886203PMC
May 2016

Levodopa-Carbidopa Intestinal Gel Infusion Therapy in Advanced Parkinson's Disease: Single Middle Eastern Center Experience.

Eur Neurol 2015 1;74(5-6):227-36. Epub 2015 Dec 1.

Movement Disorder Program, Division of Neurology, Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1159/000442151DOI Listing
August 2016

Clinical and genetic features of anoctaminopathy in Saudi Arabia.

Neurosciences (Riyadh) 2015 Apr;20(2):173-7

Department of Neurosciences, MBC 76, King Faisal Specialist Hospital & Research Centre, PO Box 3354, Riyadh 11211, Kingdom of Saudi Arabia. E-mail:

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727640PMC
http://dx.doi.org/10.17712/nsj.2015.2.20140547DOI Listing
April 2015

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Cell Rep 2015 Jan 31;10(2):148-61. Epub 2014 Dec 31.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh 11442, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2014.12.015DOI Listing
January 2015

Oromandibular dystonia in yemeni patients with khat chewing: a response to botulinum toxin treatment.

Neurol Int 2014 Apr 3;6(2):5385. Epub 2014 Jun 3.

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre , Riyadh, Saudi Arabia.

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http://dx.doi.org/10.4081/ni.2014.5385DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077212PMC
April 2014

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

Neuromuscul Disord 2014 Apr 4;24(4):353-9. Epub 2014 Jan 4.

Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Saudi Arabia; Department of Neuroscience, King Faisal Specialist Hospital and Research Centre, Saudi Arabia.

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http://dx.doi.org/10.1016/j.nmd.2013.12.010DOI Listing
April 2014

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

Gene 2014 Feb 4;536(1):217-20. Epub 2013 Dec 4.

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.gene.2013.11.043DOI Listing
February 2014

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

Eur J Hum Genet 2014 May 2;22(5):640-3. Epub 2013 Oct 2.

1] Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia [2] Laboratory of Neurogenetics, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/ejhg.2013.210DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3992572PMC
May 2014

Drug-induced Parkinson`s disease. A clinical review.

Neurosciences (Riyadh) 2013 Jul;18(3):215-21

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.

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July 2013

Multiple sclerosis in the Arabian Gulf countries: a consensus statement.

J Neurol 2013 Dec 17;260(12):2959-63. Epub 2013 Mar 17.

King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia,

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http://dx.doi.org/10.1007/s00415-013-6876-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3843364PMC
December 2013

Loss of ERLIN2 function leads to juvenile primary lateral sclerosis.

Ann Neurol 2012 Oct;72(4):510-6

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/ana.23641DOI Listing
October 2012

A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family.

Eur J Med Genet 2013 Jan 18;56(1):43-5. Epub 2012 Oct 18.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212120028
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http://dx.doi.org/10.1016/j.ejmg.2012.10.003DOI Listing
January 2013

Autosomal recessive hereditary spastic paraplegia with thin corpus callosum among Saudis.

Neurosciences (Riyadh) 2012 Jan;17(1):48-52

Departments of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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January 2012

A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia.

Hum Mutat 2012 Feb 8;33(2):351-4. Epub 2011 Dec 8.

Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/humu.21650DOI Listing
February 2012

Novel mutation of the notch3 gene in arabic family with CADASIL.

Authors:
Saeed Bohlega

Neurol Int 2011 Jul 28;3(2):e6. Epub 2011 Jul 28.

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.4081/ni.2011.e6DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3207232PMC
July 2011

A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis.

Ann Neurol 2011 Dec 12;70(6):913-9. Epub 2011 Aug 12.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://doi.wiley.com/10.1002/ana.22534
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http://dx.doi.org/10.1002/ana.22534DOI Listing
December 2011

The importance of quality-of-life assessment in the management of patients with multiple sclerosis. Recommendations from the Middle East MS Advisory Group.

Neurosciences (Riyadh) 2011 Apr;16(2):109-13

Neurology Section, King Khalid University Hospital, College of Medicine, King Saud University, PO Box 2925, Riyadh 11461, Kingdom of Saudi Arabia.

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April 2011

Clinical and molecular characterization of ataxia with oculomotor apraxia patients in Saudi Arabia.

BMC Med Genet 2011 Feb 16;12:27. Epub 2011 Feb 16.

Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riaydh, Saudi Arabia.

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http://dx.doi.org/10.1186/1471-2350-12-27DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3048493PMC
February 2011

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

Neurology 2010 Jun;74(24):e106

Department of Neurosciences and Radiology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1212/WNL.0b013e3181e3963cDOI Listing
June 2010

Primary Sjogren's syndrome with central nervous system involvement.

Saudi Med J 2009 Aug;30(8):1067-72

Department of Neurosciences, King Faisal Specialist Hospital & Research Centre, MBC 76, PO Box 3354, Riyadh 11211, Kingdom of Saudi Arabia.

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August 2009

Absence of mtDNA mutations in leukocytes of CADASIL patients.

BMC Res Notes 2008 May 30;1:16. Epub 2008 May 30.

Mitochondrial Research Laboratory, Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1186/1756-0500-1-16DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2518270PMC
May 2008

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs.

Saudi Med J 2008 Jul;29(7):952-6

Department of Neurosciences, King Faisal Specialist Hospital & Research Centre, PO Box 3354, MBC 76, Riyadh 11211, Kingdom of Saudi Arabia.

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July 2008

CADASIL in Arabs: clinical and genetic findings.

BMC Med Genet 2007 Nov 9;8:67. Epub 2007 Nov 9.

Department of Neurosciences, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1186/1471-2350-8-67DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2190758PMC
November 2007

Pan-Arab consensus statement on the use of botulinum toxin type A in spasticity management.

Neurosciences (Riyadh) 2007 Oct;12(4):279-81

Department of Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Kingdom of Saudi Arabia. Tel. +966 (1) 464 7272. Ext. 32772. Fax. +966 (1) 442 4763. E-mail:

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October 2007

Autosomal-recessive syndrome with alopecia, hypogonadism, progressive extra-pyramidal disorder, white matter disease, sensory neural deafness, diabetes mellitus, and low IGF1.

Am J Med Genet A 2007 Jan;143A(2):149-60

Department of Neurosciences, King Faisal Specialist Hospital & Research Centre, Riyadh, Kingdom of Saudi Arabia.

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http://doi.wiley.com/10.1002/ajmg.a.31497
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http://dx.doi.org/10.1002/ajmg.a.31497DOI Listing
January 2007

T313M PINK1 mutation in an extended highly consanguineous Saudi family with early-onset Parkinson disease.

Arch Neurol 2006 Oct;63(10):1483-5

Departments of Comparative Medicine and Neuroscience, and Aragene Laboratory, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://archneur.jamanetwork.com/article.aspx?doi=10.1001/arc
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http://dx.doi.org/10.1001/archneur.63.10.1483DOI Listing
October 2006

Unilateral pallidotomy for hemidystonia.

Mov Disord 2006 Jun;21(6):852-5

Division of Neurosurgery, Division of Neurology, Department of Neurosciences, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1002/mds.20838DOI Listing
June 2006

Mitochondrial T9957C mutation in association with NAION and seizures but not MELAS.

Ophthalmic Genet 2005 Mar;26(1):31-6

Department of Genetics, King Faisal Specialist Hospital and Research Centre (MBC-03), P.O. Box 3354, Riyadh 11211, Saudi Arabia.

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http://dx.doi.org/10.1080/13816810590918235DOI Listing
March 2005

Neurobrucellosis: clinical and neuroimaging correlation.

AJNR Am J Neuroradiol 2004 Mar;25(3):395-401

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, PO Box 3354, Riyadh 11211, Saudi Arabia.

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March 2004

Mutations in NHLRC1 cause progressive myoclonus epilepsy.

Nat Genet 2003 Oct 7;35(2):125-7. Epub 2003 Sep 7.

Program in Genetics and Genomic Biology, Research Institute, The Hospital for Sick Children, 555 University Avenue, Toronto, Ontario M5G 1X8, Canada.

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http://dx.doi.org/10.1038/ng1238DOI Listing
October 2003

Polyradiculopathy. A rare complication of neurobrucellosis.

Neurosciences (Riyadh) 2003 Jan;8(1):46-9

Department of Neurosciences, King Faisal Specialist Hospital and Research Centre, Riyadh, Kingdom of Saudi Arabia.

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January 2003