Diabetes Nutrition Metabolism Genetics

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    • Volume 17 Sup 1 - 2020
    • Volume 17.2 - Dec 2019
    • Volume 17.1 - Sep 2019
    • Volume 16.4 - June 2019
    • Volume 16 sup 2 - May 2019
    • Volume 16.3 - Mar 2019
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    • Volume 15.4 - Jun 2018
    • Volume 15.3 - Mar 2018
    • Volume 15.2 - Dec 2017
    • Volume 15 Sup 1 - 2017
    • Volume 15.1 - Sep 2017
    • Volume 14 Sup 2 - 2017
    • Volume 14 Sup 1 - 2017
    • Volume 14.4 - Jun 2017
    • Volume 14.3 - Mar 2017
    • Volume 14.2 - Dec 2016
    • Volume 14.1 - Sep 2016
    • Volume 13 Sup 1 - 2016
    • Volume 13.4 - Jun 2016
    • Volume 13.3 - Mar 2016
    • Volume 13.2 - Dec 2015
    • Volume 13.1 - Sep 2015
    • Volume 12.4 - Jun 2015
    • Volume 12.3 - Mar 2015
    • Volume 12.2 - Dec 2014
    • Volume 12 Sup 1 - 2014
    • Volume 12.1 - Sep 2014
    • Volume 11.4 - Jun 2014
    • Volume 11.3 - Mar 2014
    • Volume 11.2 - Dec 2013
    • Volume 11.1 - Sep 2013
    • Volume 11 Sup 2 - 2014
    • Volume 11 Sup 1 - 2014
    • Volume 10.4 - Jun 2013
    • Volume 10.3 - Mar 2013
    • Volume 10.2 - Dec 2012
    • Volume 10.1 - Sep 2012
    • Volume 10 Sup 1 - 2012
    • Volume 10 Sup 2 - 2013
    • Volume 9.4 - Jun 2012
    • Volume 9.3 - Mar 2012
    • Volume 9.2 - Dec 2011
    • Volume 9.1 - Sep 2011
    • Volume 9 Sup 2 - 2012
    • Volume 9 Sup 1 - 2011
    • Volume 8.4 - Jun 2011
    • Volume 8.3 - Mar 2011
    • Volume 8.2 - Dec 2011
    • Volume 8.1 - Sep 2010
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    Publisher: YS Medical Media Ltd. PO Box 8214, Netanya 42504, Israel. Call Us: +972-9-8641111   /   per@medmedia.co.il   /   www.medmedia.co.il/per

    • HOME

      • PES member registration
      • JSPE member registration
      • SEEP member registration
      • APEG member registration
      • SLEP member login
      • Sub vol 17 sup 1
      • Sub Vol 17.1

    • ABOUT PER

      • Editors and Editorial Board

    • Journals

      • Volume 17 Sup 1 - 2020
      • Volume 17.2 - Dec 2019
      • Volume 17.1 - Sep 2019
      • Volume 16.4 - June 2019
      • Volume 16 sup 2 - May 2019
      • Volume 16.3 - Mar 2019
      • Volume 16.2 - Dec 2018
      • Volume 16 sup 1 - 2018
      • Volume 16.1 - Sep 2018
      • Volume 15.4 - Jun 2018
      • Volume 15.3 - Mar 2018
      • Volume 15.2 - Dec 2017
      • Volume 15 Sup 1 - 2017
      • Volume 15.1 - Sep 2017
      • Volume 14 Sup 2 - 2017
      • Volume 14 Sup 1 - 2017
      • Volume 14.4 - Jun 2017
      • Volume 14.3 - Mar 2017
      • Volume 14.2 - Dec 2016
      • Volume 14.1 - Sep 2016
      • Volume 13 Sup 1 - 2016
      • Volume 13.4 - Jun 2016
      • Volume 13.3 - Mar 2016
      • Volume 13.2 - Dec 2015
      • Volume 13.1 - Sep 2015
      • Volume 12.4 - Jun 2015
      • Volume 12.3 - Mar 2015
      • Volume 12.2 - Dec 2014
      • Volume 12 Sup 1 - 2014
      • Volume 12.1 - Sep 2014
      • Volume 11.4 - Jun 2014
      • Volume 11.3 - Mar 2014
      • Volume 11.2 - Dec 2013
      • Volume 11.1 - Sep 2013
      • Volume 11 Sup 2 - 2014
      • Volume 11 Sup 1 - 2014
      • Volume 10.4 - Jun 2013
      • Volume 10.3 - Mar 2013
      • Volume 10.2 - Dec 2012
      • Volume 10.1 - Sep 2012
      • Volume 10 Sup 1 - 2012
      • Volume 10 Sup 2 - 2013
      • Volume 9.4 - Jun 2012
      • Volume 9.3 - Mar 2012
      • Volume 9.2 - Dec 2011
      • Volume 9.1 - Sep 2011
      • Volume 9 Sup 2 - 2012
      • Volume 9 Sup 1 - 2011
      • Volume 8.4 - Jun 2011
      • Volume 8.3 - Mar 2011
      • Volume 8.2 - Dec 2011
      • Volume 8.1 - Sep 2010
      • Volume 8 Sup 2 - 2011
      • Volume 8 Sup 1 - 2010
      • Previous Editions

    • Information

      • Subscribe
      • Citations
      • Submissions
      • Meetings

    • Contact Us

    • Volume 17 Sup 1 - shop

    • Volume 17.2 - shop

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      © 2017 by MEDICALMEDIA for PER Pediatric Endocrinology Reviews. All rights reserved

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      Pediatric Endocrinology Reviews (PER) is the most respected international peer reviewed journal in Pediatric Diabetes, Nutrition Metabolism and Genetics. Hypothyriodism, Hyperthyriodism, Glycemic Management for Children with Diabetes Glucose Monitoring Adrenal Insufficiency Turner Syndrome Late Adolescence Klinefelter Syndrome Children with Short Stature and Growth Failure: Heightism Type 1 Diabetes in Children Growth Hormone Treatment for GHD Insulin-like Growth Factor-I Growth Hormone Deficiency SGA Children with Short Stature Receiving GH Treatment Hypothalamic Obesity Adolescent Gynecomastia Hematospermia in Adolescents Gain-of-Function CDKN1C Mutations Craniopharyngioma Succinate-Dehydrogenase Deficient Paragangliomas/Pheochromocytomas Adrenal Steroidogenesis: Impact on Gonadal Function Focal Congenital Hyperinsulinism (CHI)  Longevity Hormone Klotho Pediatric Congenital Hypothyroid Lysosomal Storage Diseases Juvenile NCL (CLN3 Disease) GM1 and GM2 Gangliosidoses Types A and B Niemann-Pick Disease CLN2 Disease (Classic Late Infantile Neuronal Ceroid Lipofuscinosis) Krabbe Disease Fucosidosis Nuclear Factor Kappa B (NF-κB) in Growth Plate Chondrogenesis Persistent Müllerian Duct Syndrome LHX4 Gene Alterations Stunted Growth 45,X/46,XY Gonadal Dysgenesis Thyroid Hemiagenesis Nutrimetabolomics and Adipocitokines Chromosomal Microarray Analysis (CMA) Chromosomal microarray, Copy Number Variant (CNV), Prenatal, Amniocentesis, Comparative genomic hybridization, SNP array, Diagnosis, Clinical Abreviations: aCGH – array-based comparative genomic hybridization, ASD – autism spectrum disorder, BAC – bacterial artificial chromosome, CHD – congenital heart disease, CMA – chromosomal microarray analysis, CNV – copy number variant, CVS – chorionic villus sampling, DD – developmental delay, DNA – deoxyribonucleic acid, FISH – fluorescent in situ hybridization, GABA - gammaaminobutyric acid, ID – intellectual disability, LOH – loss of heterozygosity, NGS – next generation sequencing, NIPT – noninvasive prenatal testing, NOS – not otherwise specified, PGD - preimplantation genetic diagnosis, SNP – single nucleotide polymorphism, VUS – variant of unclear clinical significance Central precocious puberty, Traumatic brain injury, Pathophysiology Nephrolithiasis, Nephrocalcinosis, Hypercalciuria, Hyperoxaluria, Hypouricemia, Cystinuria, Genetics