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Mutaz Idrees Sultan

Observed names: M Sultan, Mutaz I M Sultan, Mutaz I Sultan, Mutaz I. Sultan, Mutaz Sultan, Sultan, Mutaz
ORCID: 0000-0002-1797-8772
Observed ORCID: 0000-0002-1797-8772
OpenAlex ID: A5001382662
Genetic Prevalence and Characteristics in Children With Recurrent Pancreatitis
2011 · Mutaz Sultan, Steven Werlin, et al. · Journal of Pediatric Gastroenterology and Nutrition · 69
Organic solute transporter‐β (SLC51B) deficiency in two brothers with congenital diarrhea and features of cholestasis
2017 · Mutaz Sultan, Anuradha Rao, et al. · Hepatology · 65
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Calprotectin in Cystic Fibrosis
2014 · Nisreen Rumman, Mutaz Sultan, et al. · BMC Pediatrics · 51
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H Syndrome: Recently Defined Genodermatosis With Distinct Histologic Features. A Morphological, Histochemical, Immunohistochemical, and Ultrastructural Study of 10 Cases
2010 · Victoria Doviner, Alexander Maly, et al. · American Journal of Dermatopathology · 49
Subjective Global Nutritional Assessment in Critically Ill Children
2012 · Sarah Vermilyea, Julie Slicker, et al. · Journal of Parenteral and Enteral Nutrition · 48
Endoscopic Diagnosis of Pediatric Acute Gastrointestinal Graft‐Versus‐Host Disease
2012 · Mutaz Sultan, Jonathan Ramprasad, et al. · Journal of Pediatric Gastroenterology and Nutrition · 44
One-day bowel preparation with polyethylene glycol 3350: an effective regimen for colonoscopy in children
2010 · Tonya Adamiak, Muhammad Altaf, et al. · Gastrointestinal Endoscopy · 38
Role of Nutrition in Pediatric Chronic Liver Disease
2011 · Mutaz I. Sultan, Carly D. G. Leon, et al. · Nutrition in Clinical Practice · 32
RIPK1 mutations causing infantile-onset IBD with inflammatory and fistulizing features
2022 · Mutaz Sultan, Mohammad Adawi, et al. · Frontiers in Immunology · 25
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ECCO consensus on management of inflammatory bowel disease in low- and middle-income countries
2025 · Alaa El-Hussuna, Almuthe Christina Hauer, et al. · Journal of Crohn s and Colitis · 22
Tricho‐hepato‐enteric syndrome: A case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality
2007 · Imad Dweikat, Mutaz Sultan, et al. · American Journal of Medical Genetics Part A · 20
Management of pediatric inflammatory bowel diseases in limited‐resource settings: A position paper from the Paediatric IBD Porto Group of ESPGHAN
2025 · Almuthe Christine Hauer, Mutaz Sultan, et al. · Journal of Pediatric Gastroenterology and Nutrition · 16
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Homozygous variant in MADD, encoding a Rab guanine nucleotide exchange factor, results in pleiotropic effects and a multisystemic disorder
2021 · Bassam Abu-Libdeh, Hagar Mor-Shaked, et al. · European Journal of Human Genetics · 13
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Palestinian doctors’ views on patient-centered care in hospitals
2018 · Wasim I M Sultan, Mutaz I M Sultan, et al. · BMC Health Services Research · 13
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Successful Treatment of Autoimmune Hepatitis With Methotrexate
2011 · Mutaz I Sultan, Vincent F Biank, et al. · Journal of Pediatric Gastroenterology and Nutrition · 13
Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation
2016 · Imad Mohammad Dweikat, Issa Shaher Alawneh, et al. · BMC Research Notes · 12
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Cecal Granular Cell Tumor
2011 · Mutaz I Sultan, Mariko Suchi, et al. · Journal of Pediatric Gastroenterology and Nutrition · 9
Severe persistent unremitting dermatitis, chronic diarrhea and hypoalbuminemia in a child; Hartnup disease in setting of celiac disease
2014 · Thomas Ciecierega, Imad Dweikat, et al. · BMC Pediatrics · 7
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Mutations in the kinesin KIF12 promote MASH in humans and mice by disrupting lipogenic enzyme turnover
2025 · Asieh Etemad, Yosuke Tanaka, et al. · The EMBO Journal · 3
Association of Helicobacter pylori Infection with Pediatric Asthma in Palestine
2025 · Alaa S. Hrizat, Amal A. Shahin, et al. · Pediatric Gastroenterology Hepatology & Nutrition · 3
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Wolfram Syndrome‐2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review
2023 · Rania Atieh, Thomas Ciecierega, et al. · JPGN Reports · 3
Pediatric Ménétrier’s Disease Triggered by Cytomegalovirus Infection: A Rare Case of Severe Hypoalbuminemia and Edema
2025 · Issa Snoubar, Tariq Alhendi, et al. · Case Reports in Pediatrics · 2
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DOP64 Pathogenic RIPK1 Mutations Cause Infantile-onset IBD with Inflammatory and Fistulizing Features
2022 · M Sultan, P Millman, et al. · Journal of Crohn s and Colitis · 2
Pancrelipase as Adjunctive Therapy in Severe SCOT Deficiency: A Case of a Novel OXCT1 Gene Deletion
2025 · Mo'ath Abu Hamdeh, Lema Jaber, et al. · JIMD Reports · 1
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Acute Deep Vein Thrombosis Presents as an Early Complication of Wilson Disease
2025 · Aseel Faroun, Roua Faroun, et al. · Cureus · 1
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Works count: 31
Citation count: 562
H-index: 13
I10-index: 16
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