Format
Sort by
Items per page

Send to

Choose Destination

Selected items

Items: 19

1.

Error occurred: cannot get document summary

PMID:
24250758

2.

Management of convulsive status epilepticus in children: an adapted clinical practice guideline for pediatricians in Saudi Arabia.

Bashiri FA, Hamad MH, Amer YS, Abouelkheir MM, Mohamed S, Kentab AY, Salih MA, Al Nasser MN, Al-Eyadhy AA, Al Othman MA, Al-Ahmadi T, Iqbal SM, Somily AM, Wahabi HA, Hundallah KJ, Alwadei AH, Albaradie RS, Al-Twaijri WA, Jan MM, Al-Otaibi F, Alnemri AM, Al-Ansary LA.

Neurosciences (Riyadh). 2017 Apr;22(2):146-155. doi: 10.17712/nsj.2017.2.20170093. No abstract available.

3.

Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy.

Ramadan W, Patel N, Anazi S, Kentab AY, Bashiri FA, Hamad MH, Jad L, Salih MA, Alsaif H, Hashem M, Faqeih E, Shamseddin HE, Alkuraya FS.

Clin Genet. 2017 Sep;92(3):327-331. doi: 10.1111/cge.12999. Epub 2017 Apr 19.

PMID:
28218389
4.
5.

Auto-immune anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis: three case reports.

Bashiri FA, Al-Rasheed AA, Hassan SM, Hamad MHA, El Khashab HY, Kentab AY, AlBadr FB, Salih MA.

Paediatr Int Child Health. 2017 Aug;37(3):222-226. doi: 10.1080/20469047.2016.1191852. Epub 2016 Jun 22.

PMID:
27329512
6.

A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.

Alazami AM, Kentab AY, Faqeih E, Mohamed JY, Alkhalidi H, Hijazi H, Alkuraya FS.

J Med Genet. 2015 Jun;52(6):400-4. doi: 10.1136/jmedgenet-2014-102964. Epub 2015 Mar 6.

PMID:
25748484
7.

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

Alazami AM, Patel N, Shamseldin HE, Anazi S, Al-Dosari MS, Alzahrani F, Hijazi H, Alshammari M, Aldahmesh MA, Salih MA, Faqeih E, Alhashem A, Bashiri FA, Al-Owain M, Kentab AY, Sogaty S, Al Tala S, Temsah MH, Tulbah M, Aljelaify RF, Alshahwan SA, Seidahmed MZ, Alhadid AA, Aldhalaan H, AlQallaf F, Kurdi W, Alfadhel M, Babay Z, Alsogheer M, Kaya N, Al-Hassnan ZN, Abdel-Salam GM, Al-Sannaa N, Al Mutairi F, El Khashab HY, Bohlega S, Jia X, Nguyen HC, Hammami R, Adly N, Mohamed JY, Abdulwahab F, Ibrahim N, Naim EA, Al-Younes B, Meyer BF, Hashem M, Shaheen R, Xiong Y, Abouelhoda M, Aldeeri AA, Monies DM, Alkuraya FS.

Cell Rep. 2015 Jan 13;10(2):148-61. doi: 10.1016/j.celrep.2014.12.015. Epub 2014 Dec 31.

8.

The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population.

Al-Qattan SM, Wakil SM, Anazi S, Alazami AM, Patel N, Shaheen R, Shamseldin HE, Hagos ST, AlDossari HM, Salih MA, El Khashab HY, Kentab AY, AlNasser MN, Bashiri FA, Kaya N, Hashem MO, Alkuraya FS.

Genet Med. 2015 Sep;17(9):719-25. doi: 10.1038/gim.2014.184. Epub 2014 Dec 11.

PMID:
25503496
9.

NECAP1 loss of function leads to a severe infantile epileptic encephalopathy.

Alazami AM, Hijazi H, Kentab AY, Alkuraya FS.

J Med Genet. 2014 Apr;51(4):224-8. doi: 10.1136/jmedgenet-2013-102030. Epub 2014 Jan 7.

PMID:
24399846
10.

The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.

Kentab AY, Hassan HH, Hamad MH, Alhumidi A.

Sudan J Paediatr. 2014;14(2):61-70.

11.

New findings in a global approach to dissect the whole phenotype of PLA2G6 gene mutations.

Salih MA, Mundwiller E, Khan AO, AlDrees A, Elmalik SA, Hassan HH, Al-Owain M, Alkhalidi HM, Katona I, Kabiraj MM, Chrast R, Kentab AY, Alzaidan H, Rodenburg RJ, Bosley TM, Weis J, Koenig M, Stevanin G, Azzedine H.

PLoS One. 2013 Oct 9;8(10):e76831. doi: 10.1371/journal.pone.0076831. eCollection 2013. Erratum in: PLoS One. 2013;8(11). doi:10.1371/annotation/cb01a74a-3330-4412-8040-2a94842420ed.

12.

Ophthalmologic observations in a patient with partial mosaic trisomy 8.

Abu-Amero KK, Kondkar AA, Salih MA, Al-Husain M, Al Shammari M, Zeidan G, Oystreck DT, Hellani AM, Kentab AY, Bosley TM.

Ophthalmic Genet. 2013 Dec;34(4):249-53. doi: 10.3109/13816810.2012.762933. Epub 2013 Feb 13.

PMID:
23406309
13.

Outcome of stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Al-Nasser MN.

Saudi Med J. 2006 Mar;27 Suppl 1:S91-6.

PMID:
16532136
14.

Moyamoya syndrome as a risk factor for stroke in Saudi children. Novel and usual associations.

Salih MA, Murshid WR, Al-Salman MM, Abdel-Gader AG, Al-Jarallah AA, Alorainy IA, Hassan HH, Kentab AY, Van Maldergem L, Othman SA, El-Desouki MI, Elgamal EA.

Saudi Med J. 2006 Mar;27 Suppl 1:S69-80.

PMID:
16532134
15.

Cardiac diseases as a risk factor for stroke in Saudi children.

Salih MA, Al-Jarallah AS, Abdel-Gader AG, Al-Jarallah AA, Al-Saadi MM, Kentab AY, Alorainy IA, Hassan HH.

Saudi Med J. 2006 Mar;27 Suppl 1:S61-8.

PMID:
16532133
16.

Congenital and genetic cerebrovascular anomalies as risk factors for stroke in Saudi children.

Salih MA, Murshid WR, Zahraa JN, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Tjan GT.

Saudi Med J. 2006 Mar;27 Suppl 1:S53-60.

PMID:
16532132
17.

Infectious and inflammatory disorders of the circulatory system as risk factors for stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Gadelrab MO, Alorainy IA, Hassan HH, Zahraa JN.

Saudi Med J. 2006 Mar;27 Suppl 1:S41-52.

PMID:
16532131
18.

Perinatal stroke in Saudi children. Clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Al-Nasser MN.

Saudi Med J. 2006 Mar;27 Suppl 1:S35-40.

PMID:
16532129
19.

Hematologic risk factors for stroke in Saudi children.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Murshid WR, El-Hazmi MA, Khoja WA.

Saudi Med J. 2006 Mar;27 Suppl 1:S21-34.

PMID:
16532128
20.

Stroke in Saudi children. Epidemiology, clinical features and risk factors.

Salih MA, Abdel-Gader AG, Al-Jarallah AA, Kentab AY, Alorainy IA, Hassan HH, Bahakim HM, Kurbaan KM, Zahraa JN, Al-Nasser MN, Nasir AA, Khoja WA, Kabiraj MM.

Saudi Med J. 2006 Mar;27 Suppl 1:S12-20.

PMID:
16532126

Supplemental Content

Support Center