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Results: 1 to 20 of 59

1.

Congenital toxoplasmosis presenting as central diabetes insipidus in an infant: a case report.

Mohamed S, Osman A, Al Jurayyan NA, Al Nemri A, Salih MA.

BMC Res Notes. 2014 Mar 28;7:184. doi: 10.1186/1756-0500-7-184.

PMID:
24674575
[PubMed - in process]
Free PMC Article
2.

Factors underlying inadequate parents' awareness regarding pediatrics immunization: findings of cross-sectional study in Mosul- Iraq.

Al-lela OQ, Bahari MB, Salih MR, Al-Abbassi MG, Elkalmi RM, Jamshed SQ.

BMC Pediatr. 2014 Jan 31;14:29. doi: 10.1186/1471-2431-14-29.

PMID:
24485194
[PubMed - in process]
Free PMC Article
3.

Are parents' knowledge and practice regarding immunization related to pediatrics' immunization compliance? a mixed method study.

Qutaiba B Al-lela O, Bahari MB, Al-Qazaz HK, Salih MR, Jamshed SQ, Elkalmi RM.

BMC Pediatr. 2014 Jan 25;14:20. doi: 10.1186/1471-2431-14-20.

PMID:
24460878
[PubMed - in process]
Free PMC Article
4.

Rationale and design of the DIPAK 1 study: a randomized controlled clinical trial assessing the efficacy of lanreotide to Halt disease progression in autosomal dominant polycystic kidney disease.

Meijer E, Drenth JP, d'Agnolo H, Casteleijn NF, de Fijter JW, Gevers TJ, Kappert P, Peters DJ, Salih M, Soonawala D, Spithoven EM, Torres VE, Visser FW, Wetzels JF, Zietse R, Gansevoort RT; DIPAK Consortium.

Am J Kidney Dis. 2014 Mar;63(3):446-55. doi: 10.1053/j.ajkd.2013.10.011. Epub 2013 Dec 15.

PMID:
24342522
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

CD20, CD3, placental malaria infections and low birth weight in an area of unstable malaria transmission in Central Sudan.

Batran SE, Salih MM, Elhassan EM, Mohmmed AA, Adam I.

Diagn Pathol. 2013 Nov 18;8:189. doi: 10.1186/1746-1596-8-189.

PMID:
24245949
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

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):e76831.

PMID:
24130795
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Mutations in FBXL4, encoding a mitochondrial protein, cause early-onset mitochondrial encephalomyopathy.

Gai X, Ghezzi D, Johnson MA, Biagosch CA, Shamseldin HE, Haack TB, Reyes A, Tsukikawa M, Sheldon CA, Srinivasan S, Gorza M, Kremer LS, Wieland T, Strom TM, Polyak E, Place E, Consugar M, Ostrovsky J, Vidoni S, Robinson AJ, Wong LJ, Sondheimer N, Salih MA, Al-Jishi E, Raab CP, Bean C, Furlan F, Parini R, Lamperti C, Mayr JA, Konstantopoulou V, Huemer M, Pierce EA, Meitinger T, Freisinger P, Sperl W, Prokisch H, Alkuraya FS, Falk MJ, Zeviani M.

Am J Hum Genet. 2013 Sep 5;93(3):482-95. doi: 10.1016/j.ajhg.2013.07.016. Epub 2013 Aug 29.

PMID:
23993194
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Small bowel gastrointestinal tumour: An interesting case of presentation, diagnosis and treatment.

Sofos S, Dimitrakakis G, Blake P, Pericleous A, Jackson DS, Salih M.

JRSM Short Rep. 2013 Jun 5;4(7):1-3. doi: 10.1177/2042533313481214. Print 2013 Jul. No abstract available.

PMID:
23885298
[PubMed]
Free PMC Article
9.

Submicroscopic Plasmodium falciparum malaria and low birth weight in an area of unstable malaria transmission in Central Sudan.

Mohammed AH, Salih MM, Elhassan EM, Mohmmed AA, Elzaki SE, El-Sayed BB, Adam I.

Malar J. 2013 May 28;12(1):172. [Epub ahead of print]

PMID:
23714259
[PubMed - as supplied by publisher]
Free PMC Article
10.

Mutations in B3GALNT2 cause congenital muscular dystrophy and hypoglycosylation of α-dystroglycan.

Stevens E, Carss KJ, Cirak S, Foley AR, Torelli S, Willer T, Tambunan DE, Yau S, Brodd L, Sewry CA, Feng L, Haliloglu G, Orhan D, Dobyns WB, Enns GM, Manning M, Krause A, Salih MA, Walsh CA, Hurles M, Campbell KP, Manzini MC; UK10K Consortium, Stemple D, Lin YY, Muntoni F.

Am J Hum Genet. 2013 Mar 7;92(3):354-65. doi: 10.1016/j.ajhg.2013.01.016. Epub 2013 Feb 28.

PMID:
23453667
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.

Cossins J, Belaya K, Hicks D, Salih MA, Finlayson S, Carboni N, Liu WW, Maxwell S, Zoltowska K, Farsani GT, Laval S, Seidhamed MZ; WGS500 Consortium, Donnelly P, Bentley D, McGowan SJ, Müller J, Palace J, Lochmüller H, Beeson D.

Brain. 2013 Mar;136(Pt 3):944-56. doi: 10.1093/brain/awt010. Epub 2013 Feb 11.

PMID:
23404334
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Characteristics of seizure frequency among Malaysian children diagnosed with structural-metabolic epilepsy.

Salih MR, Bahari MB, Hassali MA, Shafie AA, Al-Lela OQ, Abd AY, Ganesan VM.

J Neurosci Rural Pract. 2012 Sep;3(3):244-50. doi: 10.4103/0976-3147.102596.

PMID:
23188969
[PubMed]
Free PMC Article
13.

Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia.

Tesson C, Nawara M, Salih MA, Rossignol R, Zaki MS, Al Balwi M, Schule R, Mignot C, Obre E, Bouhouche A, Santorelli FM, Durand CM, Oteyza AC, El-Hachimi KH, Al Drees A, Bouslam N, Lamari F, Elmalik SA, Kabiraj MM, Seidahmed MZ, Esteves T, Gaussen M, Monin ML, Gyapay G, Lechner D, Gonzalez M, Depienne C, Mochel F, Lavie J, Schols L, Lacombe D, Yahyaoui M, Al Abdulkareem I, Zuchner S, Yamashita A, Benomar A, Goizet C, Durr A, Gleeson JG, Darios F, Brice A, Stevanin G.

Am J Hum Genet. 2012 Dec 7;91(6):1051-64. doi: 10.1016/j.ajhg.2012.11.001. Epub 2012 Nov 21.

PMID:
23176821
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

An incidentally discovered asymptomatic para-aortic paraganglioma with Peutz-Jeghers syndrome.

Butt N, Salih M, Khan MR, Ahmed R, Haider Z, Shah SH.

Saudi J Gastroenterol. 2012 Nov-Dec;18(6):388-91. doi: 10.4103/1319-3767.103432.

PMID:
23150026
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

A novel syndrome of lethal familial hyperekplexia associated with brain malformation.

Seidahmed MZ, Salih MA, Abdulbasit OB, Shaheed M, Al Hussein K, Miqdad AM, Al Rasheed AK, Alazami AM, Alorainy IA, Alkuraya FS.

BMC Neurol. 2012 Oct 27;12:125. doi: 10.1186/1471-2377-12-125.

PMID:
23101555
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Exome sequencing and functional validation in zebrafish identify GTDC2 mutations as a cause of Walker-Warburg syndrome.

Manzini MC, Tambunan DE, Hill RS, Yu TW, Maynard TM, Heinzen EL, Shianna KV, Stevens CR, Partlow JN, Barry BJ, Rodriguez J, Gupta VA, Al-Qudah AK, Eyaid WM, Friedman JM, Salih MA, Clark R, Moroni I, Mora M, Beggs AH, Gabriel SB, Walsh CA.

Am J Hum Genet. 2012 Sep 7;91(3):541-7. doi: 10.1016/j.ajhg.2012.07.009.

PMID:
22958903
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy.

Poduri A, Chopra SS, Neilan EG, Elhosary PC, Kurian MA, Meyer E, Barry BJ, Khwaja OS, Salih MA, Stödberg T, Scheffer IE, Maher ER, Sahin M, Wu BL, Berry GT, Walsh CA, Picker J, Kothare SV.

Epilepsia. 2012 Aug;53(8):e146-50. doi: 10.1111/j.1528-1167.2012.03538.x. Epub 2012 Jun 12.

PMID:
22690784
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Irritable bowel syndrome and psychiatric disorders in pakistan: a case control study.

Butt AS, Salih M, Jafri W, Yakoob J, Wasay M, Hamid S.

Gastroenterol Res Pract. 2012;2012:291452. doi: 10.1155/2012/291452. Epub 2012 Feb 28.

PMID:
22505882
[PubMed]
Free PMC Article
19.

Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations.

Perrault I, Saunier S, Hanein S, Filhol E, Bizet AA, Collins F, Salih MA, Gerber S, Delphin N, Bigot K, Orssaud C, Silva E, Baudouin V, Oud MM, Shannon N, Le Merrer M, Roche O, Pietrement C, Goumid J, Baumann C, Bole-Feysot C, Nitschke P, Zahrate M, Beales P, Arts HH, Munnich A, Kaplan J, Antignac C, Cormier-Daire V, Rozet JM.

Am J Hum Genet. 2012 May 4;90(5):864-70. doi: 10.1016/j.ajhg.2012.03.006. Epub 2012 Apr 12.

PMID:
22503633
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Frequency of mutations in the genes associated with hereditary sensory and autonomic neuropathy in a UK cohort.

Davidson G, Murphy S, Polke J, Laura M, Salih M, Muntoni F, Blake J, Brandner S, Davies N, Horvath R, Price S, Donaghy M, Roberts M, Foulds N, Ramdharry G, Soler D, Lunn M, Manji H, Davis M, Houlden H, Reilly M.

J Neurol. 2012 Aug;259(8):1673-85.

PMID:
22302274
[PubMed - indexed for MEDLINE]
Free PMC Article

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