Works matching IS 0334018X AND DT 2013 AND VI 26 AND IP 1/2
Results: 35
Conn syndrome and Crohn disease in a pediatric case: an interesting parallel.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 155, doi. 10.1515/jpem-2012-0033
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- Article
Adolescent ischemic stroke associated with anabolic steroid and cannabis abuse.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 161, doi. 10.1515/jpem-2012-0057
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- Article
Congenital hypothyroidism caused by a novel mutation of the dual oxidase 2 ( DUOX2) gene.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 45, doi. 10.1515/jpem-2012-0082
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Ceramide mediates inhibition of the Akt/eNOS pathway by high levels of glucose in human vascular endothelial cells.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 31, doi. 10.1515/jpem-2012-0144
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Early occurrence of cerebral white matter abnormality detected in a neonate with salt-wasting congenital adrenal hyperplasia.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 13, doi. 10.1515/jpem-2012-0154
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- Article
Pentoxifylline treatment for protecting diabetic retinopaty in children with type 1 diabetes.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 19, doi. 10.1515/jpem-2012-0166
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- Article
Glucocorticoid receptor expression in whole blood with preterm infants.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 77, doi. 10.1515/jpem-2012-0170
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- Article
The effect of different nutritional states on puberty onset and the expression of hypothalamic Kiss1/kisspepetin.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 61, doi. 10.1515/jpem-2012-0188
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Anorexia nervosa in a patient with congenital adrenal hyperplasia.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 167, doi. 10.1515/jpem-2012-0193
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- Article
Absence of diabetes mellitus type 2 in obese children and adolescents in the north of Spain.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 25, doi. 10.1515/jpem-2012-0200
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Short- and middle-term continuous use of cinacalcet in children on peritoneal dialysis.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 39, doi. 10.1515/jpem-2012-0214
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Effects of a combined intervention for treating severely obese prepubertal children.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 91, doi. 10.1515/jpem-2012-0225
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- Article
Brothers with germline PTEN mutations and persistent hypoglycemia, macrocephaly, developmental delay, short stature, and coagulopathy.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 137, doi. 10.1515/jpem-2012-0227
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- Article
Differentiated thyroid carcinoma in a girl with resistance to thyroid hormone management with triiodothyroacetic acid.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 133, doi. 10.1515/jpem-2012-0230
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Trends in hospitalizations among children with type 1 diabetes in Spain, 2001-2009.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 85, doi. 10.1515/jpem-2012-0231
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DEND syndrome due to V59A mutation in KCNJ11 gene: unresponsive to sulfonylureas.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 143, doi. 10.1515/jpem-2012-0236
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Elevated visfatin levels in obese children are related to proinflammatory factors.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 111, doi. 10.1515/jpem-2012-0237
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Severe short stature due to 3-M syndrome with a novel OBSL1 gene mutation.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 147, doi. 10.1515/jpem-2012-0239
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Vitamin D levels, insulin resistance, and cardiovascular risks in very young obese children.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 97, doi. 10.1515/jpem-2012-0244
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Attempted suicide with levothyroxine in an adolescent girl.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 129, doi. 10.1515/jpem-2012-0247
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Duplication of SOX9 is not a common cause of 46,XX testicular or 46,XX ovotesticular DSD.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 191, doi. 10.1515/jpem-2012-0280
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Celiac disease and dermatitis herpetiformis in Brazilian twins: a long-term follow-up and screening of their relatives.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 71, doi. 10.1515/jpem-2012-0282
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A clinically euthyroid child with a large goiter due to a thyroglobulin gene defect: clinical features and genetic studies.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 119, doi. 10.1515/jpem-2012-0287
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Mild form of 3-methylglutaconic aciduria type IV and mutation in the TMEM70 genes.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 151, doi. 10.1515/jpem-2012-0291
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Delayed cord clamping in full-term neonates: is it time for outlining exclusion criteria?
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 187, doi. 10.1515/jpem-2012-0292
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Arginine-guanidinoacetate-creatine pathway in preterm newborns: creatine biosynthesis in newborns.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 53, doi. 10.1515/jpem-2012-0293
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Prevalence of metabolic syndrome in children and adolescents - the recent trends in South Korea.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 105, doi. 10.1515/jpem-2012-0294
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Immune thrombocytopenic purpura in a child with thyroid hormone resistance - a rare presentation.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 125, doi. 10.1515/jpem-2012-0298
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Severe hypothalamopituitary dysfunction accompanied by influenza-associated encephalopathy: report of two pediatric cases.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 173, doi. 10.1515/jpem-2012-0304
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And what about cord blood cardiac troponin I (cTnI) levels as an inclusion criterion for therapeutic hypothermia after perinatal asphyxia?
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 189, doi. 10.1515/jpem-2012-0305
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Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 1, doi. 10.1515/jpem-2012-0327
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Octreotide-induced hepatitis in a child with persistent hyperinsulinemia hypoglycemia of infancy.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 179, doi. 10.1515/jpem-2012-0349
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Association of the interferon-γ (IFN-γ) gene polymorphism with endometriosis: is epidermal growth factor (EGF) the key-mediator?
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 193, doi. 10.1515/jpem-2012-0361
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Hepatitis in an infant treated with octreotide for congenital hyperinsulinism.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. 183, doi. 10.1515/jpem-2012-0372
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Masthead.
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- Journal of Pediatric Endocrinology & Metabolism, 2013, v. 26, n. 1/2, p. i, doi. 10.1515/jpem-2013-masthead1-2
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- Article