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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 1
1987 1
1988 3
1989 1
1990 1
1991 2
1992 3
1994 5
1995 3
1996 1
1997 2
1998 2
1999 4
2000 3
2001 4
2002 2
2003 2
2004 4
2005 3
2006 4
2007 3
2008 3
2009 2
2010 3
2011 1
2012 1
2013 5
2014 2
2015 3
2016 3
2017 8
2018 4
2019 5
2020 5
2021 6
2022 5
2023 4
2024 0

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104 results

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Page 1
Gastroesophageal reflux disease (GERD) in children.
Poddar U. Poddar U. Paediatr Int Child Health. 2019 Feb;39(1):7-12. doi: 10.1080/20469047.2018.1489649. Epub 2018 Aug 6. Paediatr Int Child Health. 2019. PMID: 30080479 Review.
Conversely, the prevalence of GERD increases with age and, by adolescence, is similar to that in adults (20%). While GER in infancy does not require investigation or therapy, an empirical proton pump inhibitor (PPI) for 4-8 weeks is justified in older children with classic …
Conversely, the prevalence of GERD increases with age and, by adolescence, is similar to that in adults (20%). While GER in infancy d …
Understanding gastroesophageal reflux disease in children.
Friedman C, Sarantos G, Katz S, Geisler S. Friedman C, et al. JAAPA. 2021 Feb 1;34(2):12-18. doi: 10.1097/01.JAA.0000731488.99461.39. JAAPA. 2021. PMID: 33448710 Review.
The diagnosis and management of GERD remains a challenge because of its nonspecific symptomatology from infancy through adolescence. Certain presenting alarm symptoms warrant a further, more extensive workup. ...Complications may arise if GERD remains untreated, ranging fr …
The diagnosis and management of GERD remains a challenge because of its nonspecific symptomatology from infancy through adolescence. …
Prader-Willi Syndrome and Chromosome 15q11.2 BP1-BP2 Region: A Review.
Butler MG. Butler MG. Int J Mol Sci. 2023 Feb 21;24(5):4271. doi: 10.3390/ijms24054271. Int J Mol Sci. 2023. PMID: 36901699 Free PMC article. Review.
Prader-Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as severe hypotonia, failure to thrive, hypogonadism/hypogenitalism and developmental delay during infancy. ...
Prader-Willi syndrome (PWS) is a complex genetic disorder with three PWS molecular genetic classes and presents as severe hypotonia, fail …
Pearson syndrome: a multisystem mitochondrial disease with bone marrow failure.
Yoshimi A, Ishikawa K, Niemeyer C, Grünert SC. Yoshimi A, et al. Orphanet J Rare Dis. 2022 Oct 17;17(1):379. doi: 10.1186/s13023-022-02538-9. Orphanet J Rare Dis. 2022. PMID: 36253820 Free PMC article. Review.
Non hematological symptoms suggesting a mitochondrial disease are often lacking at initial presentation, thus PS is an important differential diagnosis in isolated hypogenerative anemia in infancy. Spontaneous resolution of anemia occurs in two-third of patients at the age …
Non hematological symptoms suggesting a mitochondrial disease are often lacking at initial presentation, thus PS is an important differentia …
Obesity in Prader-Willi syndrome: physiopathological mechanisms, nutritional and pharmacological approaches.
Muscogiuri G, Barrea L, Faggiano F, Maiorino MI, Parrillo M, Pugliese G, Ruggeri RM, Scarano E, Savastano S, Colao A; RESTARE. Muscogiuri G, et al. J Endocrinol Invest. 2021 Oct;44(10):2057-2070. doi: 10.1007/s40618-021-01574-9. Epub 2021 Apr 23. J Endocrinol Invest. 2021. PMID: 33891302 Free PMC article. Review.
The main clinical characteristics are represented by short stature, developmental delay, cognitive disability and behavioral diseases. Hypotonia and poor suck resulting in failure to thrive are typical of infancy. As the subjects with PWS age, clinical …
The main clinical characteristics are represented by short stature, developmental delay, cognitive disability and behavioral diseases. Hypot …
Prader-Willi syndrome: a review of clinical, genetic, and endocrine findings.
Angulo MA, Butler MG, Cataletto ME. Angulo MA, et al. J Endocrinol Invest. 2015 Dec;38(12):1249-63. doi: 10.1007/s40618-015-0312-9. Epub 2015 Jun 11. J Endocrinol Invest. 2015. PMID: 26062517 Free PMC article. Review.
Clinical manifestations change with age with hypotonia and a poor suck resulting in failure to thrive during infancy. As the individual ages, other features such as short stature, food seeking with excessive weight gain, developmental delay, cognitive …
Clinical manifestations change with age with hypotonia and a poor suck resulting in failure to thrive during infancy …
Diencephalic syndrome in childhood, a challenging cause of failure to thrive: miniseries and literature review.
Trapani S, Bortone B, Bianconi M, Rubino C, Sardi I, Lionetti P, Indolfi G. Trapani S, et al. Ital J Pediatr. 2022 Aug 17;48(1):147. doi: 10.1186/s13052-022-01316-4. Ital J Pediatr. 2022. PMID: 35978327 Free PMC article. Review.
The aim of our study was to better define the clinical pattern of diencephalic syndrome, a rare but potentially lethal cause of failure to thrive in infancy. Poor weight gain or weight loss, the characteristic presenting feature, often firstly attribut …
The aim of our study was to better define the clinical pattern of diencephalic syndrome, a rare but potentially lethal cause of failure …
Biliary atresia.
Mieli-Vergani G, Vergani D. Mieli-Vergani G, et al. Semin Immunopathol. 2009 Sep;31(3):371-81. doi: 10.1007/s00281-009-0171-6. Epub 2009 Jun 17. Semin Immunopathol. 2009. PMID: 19533128 Review.
Biliary atresia (BA) is a condition unique to infancy. It results from inflammatory destruction of the intrahepatic and extrahepatic bile ducts. ...Clinical presentation is in the first few weeks of life with conjugated hyperbilirubinaemia (dark urine and pale stools); oth …
Biliary atresia (BA) is a condition unique to infancy. It results from inflammatory destruction of the intrahepatic and extrahepatic …
Syndromic diarrhea/Tricho-hepato-enteric syndrome.
Fabre A, Martinez-Vinson C, Goulet O, Badens C. Fabre A, et al. Orphanet J Rare Dis. 2013 Jan 9;8:5. doi: 10.1186/1750-1172-8-5. Orphanet J Rare Dis. 2013. PMID: 23302111 Free PMC article. Review.
The classical form is characterized by 5 clinical signs: intractable diarrhea of infancy beginning in the first month of life, usually leading to failure to thrive and requiring parenteral nutrition; facial dysmorphism characterised by prominent forehe …
The classical form is characterized by 5 clinical signs: intractable diarrhea of infancy beginning in the first month of life, usuall …
Food Protein-Induced Enterocolitis Syndrome.
Bingemann TA, Sood P, Järvinen KM. Bingemann TA, et al. Immunol Allergy Clin North Am. 2018 Feb;38(1):141-152. doi: 10.1016/j.iac.2017.09.009. Epub 2017 Oct 26. Immunol Allergy Clin North Am. 2018. PMID: 29132670 Review.
Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE-mediated food allergy that usually presents in infancy. Cow's milk, soy, and grains are the most common food triggers. ...
Food protein-induced enterocolitis syndrome (FPIES) is a non-IgE-mediated food allergy that usually presents in infancy. Cow's milk, …
104 results