Sultan M - Search Results

1

Homozygous variant in MADD, encoding a Rab guanine nucleotide exchange factor, results in pleiotropic effects and a multisystemic disorder.

Abu-Libdeh B, Mor-Shaked H, Atawna AA, Gillis D, Halstuk O, Shaul-Lotan N, Slae M, Sultan M, Meiner V, Elpeleg O, Harel T. Abu-Libdeh B, et al. Among authors: sultan m. Eur J Hum Genet. 2021 Jun;29(6):977-987. doi: 10.1038/s41431-021-00844-7. Epub 2021 Mar 15. Eur J Hum Genet. 2021. PMID: 33723354 Free PMC article.

2

Tricho-hepato-enteric syndrome: a case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality.

Dweikat I, Sultan M, Maraqa N, Hindi T, Abu-Rmeileh S, Abu-Libdeh B. Dweikat I, et al. Among authors: sultan m. Am J Med Genet A. 2007 Mar 15;143A(6):581-3. doi: 10.1002/ajmg.a.31583. Am J Med Genet A. 2007. PMID: 17236206

3

Organic solute transporter-β (SLC51B) deficiency in two brothers with congenital diarrhea and features of cholestasis.

Sultan M, Rao A, Elpeleg O, Vaz FM, Abu-Libdeh B, Karpen SJ, Dawson PA. Sultan M, et al. Hepatology. 2018 Aug;68(2):590-598. doi: 10.1002/hep.29516. Epub 2018 May 11. Hepatology. 2018. PMID: 28898457 Free PMC article.

4

Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation.

Dweikat IM, Alawneh IS, Bahar SF, Sultan MI. Dweikat IM, et al. BMC Res Notes. 2016 Aug 4;9:387. doi: 10.1186/s13104-016-2184-2. BMC Res Notes. 2016. PMID: 27487919 Free PMC article.

5

Severe persistent unremitting dermatitis, chronic diarrhea and hypoalbuminemia in a child; Hartnup disease in setting of celiac disease.

Ciecierega T, Dweikat I, Awar M, Shahrour M, Libdeh BA, Sultan M. Ciecierega T, et al. Among authors: sultan m. BMC Pediatr. 2014 Dec 20;14:311. doi: 10.1186/s12887-014-0311-6. BMC Pediatr. 2014. PMID: 25526748 Free PMC article.

6

One-day bowel preparation with polyethylene glycol 3350: an effective regimen for colonoscopy in children.

Adamiak T, Altaf M, Jensen MK, Sultan M, Ramprasad J, Ciecierega T, Sherry K, Miranda A. Adamiak T, et al. Among authors: sultan m. Gastrointest Endosc. 2010 Mar;71(3):573-7. doi: 10.1016/j.gie.2009.10.042. Gastrointest Endosc. 2010. PMID: 20189516

7

Calprotectin in cystic fibrosis.

Rumman N, Sultan M, El-Chammas K, Goh V, Salzman N, Quintero D, Werlin S. Rumman N, et al. Among authors: sultan m. BMC Pediatr. 2014 May 29;14:133. doi: 10.1186/1471-2431-14-133. BMC Pediatr. 2014. PMID: 24885444 Free PMC article.

8

RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing features.

Sultan M, Adawi M, Kol N, McCourt B, Adawi I, Baram L, Tal N, Werner L, Lev A, Snapper SB, Barel O, Konnikova L, Somech R, Shouval DS. Sultan M, et al. Front Immunol. 2022 Nov 18;13:1041315. doi: 10.3389/fimmu.2022.1041315. eCollection 2022. Front Immunol. 2022. PMID: 36466854 Free PMC article.

9

H syndrome: recently defined genodermatosis with distinct histologic features. A morphological, histochemical, immunohistochemical, and ultrastructural study of 10 cases.

Doviner V, Maly A, Ne'eman Z, Qawasmi R, Aamar S, Sultan M, Spiegel M, Molho-Pessach V, Zlotogorski A. Doviner V, et al. Among authors: sultan m. Am J Dermatopathol. 2010 Apr;32(2):118-28. doi: 10.1097/DAD.0b013e3181b28572. Am J Dermatopathol. 2010. PMID: 20010285

10

Cecal granular cell tumor.

Sultan MI, Suchi M, Werlin SL. Sultan MI, et al. J Pediatr Gastroenterol Nutr. 2011 Apr;52(4):375. doi: 10.1097/MPG.0b013e3181fb47b8. J Pediatr Gastroenterol Nutr. 2011. PMID: 21407113 No abstract available.

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