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Journal of the Neurological Sciences, ISSN 0022-510X, 10/2017, Volume 381, pp. 17 - 17
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2015, Volume 357, pp. e488 - e489
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 12/2019, Volume 69, pp. 99 - 103
Woodhouse–Sakati syndrome (WSS) is a rare autosomal recessive disease with characteristic neuro-endocrine manifestations. WSS encompasses heterogeneous... 
NBIA | Dystonia | Woodhouse-Sakati syndrome | Hypogonadism | MENTAL-RETARDATION | C2ORF37 | CLINICAL NEUROLOGY | FAMILY | DIABETES-MELLITUS | DISEASE | DEAFNESS | MUTATIONS | ALOPECIA
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 07/2019, Volume 64, pp. 145 - 149
ADCY5-related hyperkinesia encompasses a heterogeneous group of phenotypes, including paroxysmal chorea, myoclonus, and dystonia. The disease is attributed to... 
Adenylyl cyclase 5 | Autosomal recessive | Phenotype | Myoclonus | Genotype | Dystonia | Mutation | ADCY5 | ADCY5 MUTATIONS | MYOKYMIA | CLINICAL NEUROLOGY | FAMILIAL DYSKINESIA | CHOREA | DISEASE | DEEP BRAIN-STIMULATION | Medical research | Enzymes | Medicine, Experimental | Genetic research | Anxiety
Journal Article
Cell Reports, ISSN 2211-1247, 01/2015, Volume 10, Issue 2, pp. 148 - 161
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 10/2019, Volume 405, pp. 111 - 111
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 10/2019, Volume 405, pp. 333 - 334
Journal Article
Journal Article
Multiple Sclerosis and Related Disorders, ISSN 2211-0348, 2014, Volume 3, Issue 6, pp. 766 - 767
Multiple sclerosis (MS) is reported globally and is the most common cause of neurological disability in young adults. Comparisons of the incidence and... 
Neurology
Journal Article
by Monies, Dorota and Abouelhoda, Mohamed and AlSayed, Moeenaldeen and Alhassnan, Zuhair and Alotaibi, Maha and Kayyali, Husam and Al-Owain, Mohammed and Shah, Ayaz and Rahbeeni, Zuhair and Al-Muhaizea, Mohammad A and Alzaidan, Hamad I and Cupler, Edward and Bohlega, Saeed and Faqeih, Eissa and Faden, Maha and Alyounes, Banan and Jaroudi, Dyala and Goljan, Ewa and Elbardisy, Hadeel and Akilan, Asma and Albar, Renad and Aldhalaan, Hesham and Gulab, Shamshad and Chedrawi, Aziza and Al Saud, Bandar K and Kurdi, Wesam and Makhseed, Nawal and Alqasim, Tahani and El Khashab, Heba Y and Al-Mousa, Hamoud and Alhashem, Amal and Kanaan, Imaduddin and Algoufi, Talal and Alsaleem, Khalid and Basha, Talal A and Al-Murshedi, Fathiya and Khan, Sameena and Al-Kindy, Adila and Alnemer, Maha and Al-Hajjar, Sami and Alyamani, Suad and Aldhekri, Hasan and Al-Mehaidib, Ali and Arnaout, Rand and Dabbagh, Omar and Shagrani, Mohammad and Broering, Dieter and Tulbah, Maha and Alqassmi, Amal and Almugbel, Maisoon and AlQuaiz, Mohammed and Alsaman, Abdulaziz and Al-Thihli, Khalid and Sulaiman, Raashda A and Al-Dekhail, Wajeeh and Alsaegh, Abeer and Bashiri, Fahad A and Qari, Alya and Alhomadi, Suzan and Alkuraya, Hisham and Alsebayel, Mohammed and Hamad, Muddathir H and Szonyi, Laszlo and Abaalkhail, Faisal and Al-Mayouf, Sulaiman M and Almojalli, Hamad and Alqadi, Khalid S and Elsiesy, Hussien and Shuaib, Taghreed M and Seidahmed, Mohammed Zain and Abosoudah, Ibraheem and Akleh, Hana and AlGhonaium, Abdulaziz and Alkharfy, Turki M and Al Mutairi, Fuad and Eyaid, Wafa and Alshanbary, Abdullah and Sheikh, Farrukh R and Alsohaibani, Fahad I and Alsonbul, Abdullah and Al Tala, Saeed and Balkhy, Soher and Bassiouni, Randa and Alenizi, Ahmed S and Hussein, Maged H and Hassan, Saeed and Khalil, Mohamed and Tabarki, Brahim and Alshahwan, Saad and Oshi, Amira and Sabr, Yasser and Alsaadoun, Saad and Salih, Mustafa A and Mohamed, Sarar and Sultana, Habiba and Tamim, Abdullah and El-Haj, Moayad and Alshahrani, Saif and Bubshait, Dalal K and Alfadhel, Majid and ...
Human Genetics, ISSN 0340-6717, 8/2017, Volume 136, Issue 8, pp. 921 - 939
Journal Article
Cell death and differentiation, ISSN 1350-9047, 2017, Volume 24, Issue 10, pp. 1655 - 1671
Journal Article
Journal of Neurology, ISSN 0340-5354, 12/2013, Volume 260, Issue 12, pp. 2959 - 2963
The epidemiology of multiple sclerosis (MS) is rapidly changing in many parts of the world. Based on the Kurtzke classification, the Arabian Gulf Region is... 
Neurology | Neurosciences | Multiple sclerosis | Treatment | Medicine & Public Health | Diagnosis | Neuroradiology | Arabian Gulf | Guidelines | BENEFIT | CONSANGUINITY | PREVALENCE | SAUDI-ARABIA | EVENT | CLINICAL NEUROLOGY | Multiple Sclerosis - epidemiology | Middle East - epidemiology | Humans | Care and treatment | Relapse | Control | Prognosis | Diseases | Classification | Review
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 07/2017, Volume 8, p. 333
Journal Article
Neurology, ISSN 0028-3878, 05/2014, Volume 82, Issue 18, pp. 1665 - 1666
Anas M. Alazami, Fatema Alzahrani, Saeed Bohlega, Fowzan S. Alkuraya, Riyadh, Saudi Arabia: Nakhro et al.[1] described a compound heterozygous mutation in SET... 
MALE-INFERTILITY | CLINICAL NEUROLOGY | Humans | Female | Male | Transcriptome - genetics | Intracellular Signaling Peptides and Proteins - genetics | Mutation, Missense - genetics | Charcot-Marie-Tooth Disease - genetics
Journal Article
BMC MEDICAL GENETICS, ISSN 1471-2350, 07/2019, Volume 20, Issue 1, pp. 119 - 6
BackgroundMutations in ARL6IP1, which encodes a tetraspan membrane protein localized to the endoplasmic reticulum (ER), have been recently described in a large... 
Hereditary spastic paraplegia | ADP ribosylation factor like GTPase 6 interacting protein 1 | Autosomal recessive | Whole exome sequencing | MEMBRANE | GENETICS & HEREDITY | PROTEINS | Gene mutations | Paralysis, Spastic | Research | Medical research | Analysis | Patient outcomes | Medicine, Experimental | Infants | Seizures (Medicine)
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 5, pp. 640 - 643
Journal Article