about
Evidence of hormone resistance in a pseudo-pseudohypoparathyroidism patient with a novel paternal mutation in GNAS.Retinal Ganglion Cell Loss in Children With Type 1 Diabetes Mellitus Without Diabetic Retinopathy.Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis.Effect of iron supplementation on development of iron deficiency anemia in breastfed infants.CDH3 gene related hypotrichosis and juvenile macular dystrophy - A case with a novel mutation.Hypoglycemia is common in children with cystic fibrosis and seen predominantly in females.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.Novel homozygous inactivating mutation of the calcium-sensing receptor gene (CASR) in neonatal severe hyperparathyroidism-lack of effect of cinacalcet.Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest TurkeyHereditary 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
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Saygin Abali
@en
Saygin Abali
@nl
type
label
Saygin Abali
@en
Saygin Abali
@nl
prefLabel
Saygin Abali
@en
Saygin Abali
@nl
P31
P496
0000-0001-6552-2801