Kadhim H - Search Results

1

A novel large deletion in the RYR1 gene in a Belgian family with late-onset and recessive core myopathy.

Remiche G, Kadhim H, Abramowicz M, Mavroudakis N, Monnier N, Lunardi J. Remiche G, et al. Among authors: kadhim h. Neuromuscul Disord. 2015 May;25(5):397-402. doi: 10.1016/j.nmd.2015.01.016. Epub 2015 Feb 9. Neuromuscul Disord. 2015. PMID: 25747005

2

[Peripheral neuropathies, from diagnosis to treatment, review of the literature and lessons from the local experience].

Remiche G, Kadhim H, Maris C, Mavroudakis N. Remiche G, et al. Among authors: kadhim h. Rev Med Brux. 2013 Sep;34(4):211-20. Rev Med Brux. 2013. PMID: 24195230 Review. French.

3

Recurrent episodes of myoglobinuria, mental retardation and seizures but no hemolysis in two brothers with phosphoglycerate kinase deficiency.

Coppens S, Koralkova P, Aeby A, Mojzikova R, Deconinck N, Kadhim H, van Wijk R. Coppens S, et al. Among authors: kadhim h. Neuromuscul Disord. 2016 Mar;26(3):207-10. doi: 10.1016/j.nmd.2015.11.008. Epub 2015 Nov 30. Neuromuscul Disord. 2016. PMID: 26883264

4

Dembour A, Destrée A, Deprez M, Kadhim H, Karadurmus D, Froment O, Deconinck N, Lederer D. Dembour A, et al. Among authors: kadhim h. Eur J Med Genet. 2022 Apr;65(4):104469. doi: 10.1016/j.ejmg.2022.104469. Epub 2022 Mar 8. Eur J Med Genet. 2022. PMID: 35276412 Review.

5

A form of muscular dystrophy associated with pathogenic variants in JAG2.

Coppens S, Barnard AM, Puusepp S, Pajusalu S, Õunap K, Vargas-Franco D, Bruels CC, Donkervoort S, Pais L, Chao KR, Goodrich JK, England EM, Weisburd B, Ganesh VS, Gudmundsson S, O'Donnell-Luria A, Nigul M, Ilves P, Mohassel P, Siddique T, Milone M, Nicolau S, Maroofian R, Houlden H, Hanna MG, Quinlivan R, Beiraghi Toosi M, Ghayoor Karimiani E, Costagliola S, Deconinck N, Kadhim H, Macke E, Lanpher BC, Klee EW, Łusakowska A, Kostera-Pruszczyk A, Hahn A, Schrank B, Nishino I, Ogasawara M, El Sherif R, Stojkovic T, Nelson I, Bonne G, Cohen E, Boland-Augé A, Deleuze JF, Meng Y, Töpf A, Vilain C, Pacak CA, Rivera-Zengotita ML, Bönnemann CG, Straub V, Handford PA, Draper I, Walter GA, Kang PB. Coppens S, et al. Among authors: kadhim h. Am J Hum Genet. 2021 May 6;108(5):840-856. doi: 10.1016/j.ajhg.2021.03.020. Epub 2021 Apr 15. Am J Hum Genet. 2021. PMID: 33861953 Free PMC article.

6

Adult polyglucosan body disease masquerading as "ALS with dementia of the Alzheimer type": an exceptional phenotype in a rare pathology.

Segers K, Kadhim H, Colson C, Duttmann R, Glibert G. Segers K, et al. Among authors: kadhim h. Alzheimer Dis Assoc Disord. 2012 Jan-Mar;26(1):96-9. doi: 10.1097/WAD.0b013e31821cc65d. Alzheimer Dis Assoc Disord. 2012. PMID: 21572310

7

Early modified functional hemispherectomy in a young infant with Ohtahara syndrome and hemimegalencephaly.

Nachanakian A, Hmaimess G, El-Helou A, Alaywan M, Adem-Hachem C, Kadhim H. Nachanakian A, et al. Among authors: kadhim h. J Child Neurol. 2015 Mar;30(4):522-6. doi: 10.1177/0883073814539558. Epub 2014 Jul 14. J Child Neurol. 2015. PMID: 25028415

8

Crohn's disease-related 'gastrocnemius myalgia syndrome' successfully treated with infliximab: A case report.

Catherine J, Kadhim H, Lambot F, Liefferinckx C, Meurant V, Otero Sanchez L. Catherine J, et al. Among authors: kadhim h. World J Gastroenterol. 2022 Feb 21;28(7):755-762. doi: 10.3748/wjg.v28.i7.755. World J Gastroenterol. 2022. PMID: 35317272 Free PMC article.

9

Metachromatic leukodystrophy without arylsulfatase A deficiency: a new case of saposin-B deficiency.

Deconinck N, Messaaoui A, Ziereisen F, Kadhim H, Sznajer Y, Pelc K, Nassogne MC, Vanier MT, Dan B. Deconinck N, et al. Among authors: kadhim h. Eur J Paediatr Neurol. 2008 Jan;12(1):46-50. doi: 10.1016/j.ejpn.2007.05.004. Epub 2007 Jul 5. Eur J Paediatr Neurol. 2008. PMID: 17616409

10

Dermatomyositis Associated with Sarcoidosis: Two Cases.

Sidiras P, Vandergheynst F, Verset L, Kadhim H, Soyfoo MS. Sidiras P, et al. Among authors: kadhim h. Eur J Case Rep Intern Med. 2017 Jan 27;4(1):000500. doi: 10.12890/2016_000500. eCollection 2017. Eur J Case Rep Intern Med. 2017. PMID: 30755904 Free PMC article.

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