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CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation.

artículo científico publicado en 2017

Effect of iron supplementation on development of iron deficiency anemia in breastfed infants.

artículo científico publicado en 2012

Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS.

artículo científico publicado en 2014

Hereditary vitamin D-resistant rickets: a report of four cases with two novel variants in the VDR gene and successful use of intermittent intravenous calcium via a peripheral route

artículo científico publicado en 2020

Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females.

artículo científico publicado en 2016

Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.

artículo científico publicado en 2013

Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey

artículo científico publicado en 2018

Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.

artículo científico publicado en 2014

Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy

artículo científico publicado en 2017

The assessment of peripapillary retinal nerve fiber layer and macular ganglion cell layer changes in obese children: a cross-sectional study using optical coherence tomography.

artículo científico publicado en 2016