Volume 9.4 Shop | per-1

top of page

Diabetes Nutrition Metabolism Genetics

Pediatric Endocrinology Reviews

HOME
ABOUT PER
- Editors and Editorial Board
Journals
Information
Contact Us
Volume 17 Sup 1 - shop
Volume 17.2 - shop
More

Use tab to navigate through the menu items.

Purchase Articles

Vol. 9.4

June 2012

Choose an article to purchase

To Be Or Not To Be "TALL"? Zvi Laron, MD, PhD (h.c
Price$69.00
Can The Consequences of Universal Cholesterol Scre
Price$69.00
GLI2 Mutations as a Cause of Hypopituitarism Lauri
Price$69.00
Empty Sella Syndrome Anne M. Lenz1, MD, Allen W. R
Price$69.00
Neurocognitive Development of Children Born Small
Price$69.00
Treatment of Short Stature Due To SHOX Haploinsuff
Price$69.00
2012 Annual Meeting of Pediatric Endocrine Society
Price$69.00

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
ABOUT PER
- Editors and Editorial Board
Journals
Information
Contact Us
Volume 17 Sup 1 - shop
Volume 17.2 - shop
More

Use tab to navigate through the menu items.

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

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

bottom of page