Works matching IS 0334018X AND DT 2016 AND VI 29 AND IP 9
Results: 16
Hyperinsulinism-hyperammonemia syndrome: a de novo mutation of the GLUD1 gene in twins and a review of the literature.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1083, doi. 10.1515/jpem-2016-0086
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- Article
Hormone disorder and vitamin deficiency in attention deficit hyperactivity disorder (ADHD) and autism spectrum disorders (ASDs).
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1077, doi. 10.1515/jpem-2015-0473
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- Article
Percentiles for anthropometric measures in Iranian children and adolescents: the CASPIAN-IV study.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1069, doi. 10.1515/jpem-2016-0041
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- Article
Factors associated with post-menarcheal growth: results of a longitudinal study in Chilean girls from different socioeconomic statuses.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1063, doi. 10.1515/jpem-2016-0035
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- Article
A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1111, doi. 10.1515/jpem-2015-0482
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- Article
Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1103, doi. 10.1515/jpem-2015-0261
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- Article
Novel homozygous likely-pathogenic intronic variant in INS causing permanent neonatal diabetes in siblings.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1089, doi. 10.1515/jpem-2016-0040
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- Article
A girl with permanent neonatal diabetes due to KCNJ11 mutation presented with Mauriac syndrome after improper adjustment in sulfonylurea dosage over 6 years.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1095, doi. 10.1515/jpem-2016-0065
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- Article
Referral pattern of children with short stature to a pediatric endocrine clinic in Kuwait.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1055, doi. 10.1515/jpem-2016-0098
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- Article
Identification of monogenic gene mutations in Japanese subjects diagnosed with type 1B diabetes between > 5 and 15.1 years of age.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1047, doi. 10.1515/jpem-2016-0030
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- Article
In children with autoimmune thyroid diseases the association with Down syndrome can modify the clustering of extra-thyroidal autoimmune disorders.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1041, doi. 10.1515/jpem-2016-0073
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- Article
Pilot study of newborn screening of inborn error of metabolism using tandem mass spectrometry in Malaysia: outcome and challenges.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1031, doi. 10.1515/jpem-2016-0028
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- Article
WHO European Childhood Obesity Surveillance Initiative in Serbia: a prevalence of overweight and obesity among 6-9-year-old school children.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1025, doi. 10.1515/jpem-2016-0138
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- Article
Prevalence and awareness of functional and structural foot abnormalities in children and adolescents with type 1 diabetes.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1019, doi. 10.1515/jpem-2015-0455
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- Article
A germline mutation of HRPT2/CDC73 (70 G > T) in an adolescent female with parathyroid carcinoma: first case report and a review of the literature.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1005, doi. 10.1515/jpem-2016-0109
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- Article
Seroprotection status of hepatitis B and measles vaccines in children with type 1 diabetes mellitus.
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- Journal of Pediatric Endocrinology & Metabolism, 2016, v. 29, n. 9, p. 1013, doi. 10.1515/jpem-2015-0211
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- Article