Kalp sağlığı klinikleri şikago.
Beyoglu Eye J. Turkiye Klinikleri J Med Sci. Biol Trace Elem Res. Serum fetuin-A and insulin levels in classic congenital adrenal hyperplasia. Horm Metab Res. Turk Clin Lab. J Clin Res Pediatr E. Ocul Immunol and Inflamm.
J Pediatr Endocr Met. Vitamin D deficiency in adolescent pregnancy and obstetric outcomes. Taiwan J Obstet Gynecol. Functional assessment of variants associated with Kalp sağlığı klinikleri şikago. syndrome. Hum Mol Genet. Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations. Hum Mutat.
Experience of intravenous calcium treatment and long-term responses to treatment in a patient with hereditary vitamin D-resistant rickets resulting from a novel mutation. J Pediatr Endocrinol Metab. J Clin Endocrinol Metab. Am Uykuda tansiyon neden yükselir Ophthalmol. Evaluation of long-term follow-up and methimazole therapy outcomes of pediatric Graves' disease: a single-center experience.
J Clin Res Pediatr Endocrinol. Ocul Immunol Inflamm. Diabetes Res Clin Pract. J Gynecol Obstet Hum Reprod. Horm Res Paediatr.
Low hemoglobin A1c levels in a patient with diabetic ketoacidosis: Fulminant type 1 diabetes mellitus. Turk J Pediatr. Follow-up in children with non-obese and non-autoimmune subclinical hypothyroidism.
Near final height in patients with idiopathic growth hormone deficiency: A single-centre experience. J Paediatr Child Health. Investigation of MKRN3 mutation in patients with familial central precocious puberty. Quantitative evaluation of early retinal changes in children with type 1 diabetes mellitus without retinopathy.
Clin Exp Optom. Clinical follow-up data and them rate of development of precocious and rapidly progressive puberty in patients with premature thelarche. Response to growth hormone treatment in very young patients with growth hormone deficiencies and mini-puberty.
Evaluation of anterior segment parameters in patients with Turner syndrome using Scheimpflug imaging. Clinical and genetic characterisation of a series of patients with triple A syndrome.
Eur J Pediatr. Vaginal bleeding and a giant ovarian cyst in an infant with hydroxylase deficiency. Subclinical left ventricular systolic and diastolic dysfunction in type 1 diabetic children and adolescents with good metabolic control.
Quantitative evaluation of early retinal changes in children with Typ 1 diabetes mellitus without retinopaty. Subnormal growth velocity and related factors during GnRH analog therapy for idiopathic central precocious puberty.
Novel mutations in the LRP5 kalp sağlığı klinikleri şikago. in patients with Osteoporosis-pseudoglioma syndrome. Am J Med Genet A. Effects of 1-year growth hormone replacement therapy on thyroid volume and function of the children and adolescents with idiopathic growth hormone deficiency.
Type 1 rhizomelic chondrodysplasia punctata with a homozygous PEX7 mutation. Clinical, biochemical and genetic features with nonclassical hydroxylase deficiency and final height. The variable clinical phenotype of three patients with hepatic glycogen synthase deficiency.
AMH levels in girls with various pubertal problems.
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Conventional insulin pump therapy in two neonatal diabetes patients harboring the homozygous PTF1A enhancer mutation: Need for a novel approach for the management of neonatal diabetes. Turk J Med Sci. Bone mineral density and growth in children with coeliac disease on a gluten free-diet.
The growth characteristics of patients with Noonan syndrome, and first 3 years results of GH treatment: A Nationwide multicenter study. Comparison of anterior segment parameters in juvenile diabetes mellitus and healthy eyes. Eur J Ophthalmol.
J Pediatr Ophthalmol Strabismus. Comprehensive screening of eight known causative genes in congenital hypothyroidism kalp sağlığı klinikleri şikago.
gland-in-situ. J Clin endocrinol Metab. Gonadoblastoma in a patient with 46 XY complete gonadal dysgenesis. A case with athrophic autoimmune thyroidditis-related hypothyroidism causing multisystem involvement in early childhood. Complete androgen insensitivity syndrome associated with bilateral sertoli cell adenomas and unilateral paratesticuler leiomyoma: a case report. The firs childhood case with coexisting Hashimoto thyroiditis, vitiligo and autoimmune hepatitis.
Optic Nerve parameters in obese children as measured by spectral domain optical coherence tomography. Seminars Ophtalmology. Is chromosomal study necessary for girls with inguinal hernia?. Letter to editor. J Clin Diagn Res. Treatment experience and long term follow-up data in two severe neonatal hyperparathyroidism cases. Maturity onset diabetes of youth MODY in Turkish children: sequence analysis of 11 causative genes by next generation sequencing. Efficacy and safety of pamidronate in children with vitamin D intoxication.
Pediatr Int. Int J Endocrinol. The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism. Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets.
- Но я по крайней мере _не видел_ Кэти, - О Боже, - перебила его Николь, - я чуть не забыла.
- Prof. Dr. Erkan Doğan - Medikal Onkoloji
- YAKIN DOĞU ÜNİVERSİTESİ, AMERİKA KARDİYOLOJİ KOLEJİ KONGRESİNDE TEMSİL EDİLDİ - İstanbul Haberleri
- Мобильная камера Ричарда не обнаружила ничего нового, а на единственном нижнем уровне выхода не .
Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development. J Pediatr EndocrinolMetab. Rett syndrome and precocious pubertyassociation.
Investigation ofautoimmune diseases accompanying Hashimoto's thyroiditis in children andadolescents and evaluation of cardiac signs. Effects of GnRH analogue treatment on anterior pituitary hormones in childrenwith central precocious puberty.
The use of pamidronate for acute vitamin D intoxication, clinical experience with three cases. Y27 c.
Balkan Med J. What has national screening program changed in cases with congenital hypothyroidism? Iran J Pediatr.
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Clinical review of 95 patients with46,XX disorders of sex development based on the new Chicago classification. Kalp sağlığı klinikleri şikago. Adolesc Gynecol.
Uluslararası hakemli dergilerde yayımlanan makaleler:.
Approach to thyroid nodules in children and adolescents. An uncommon cause of hypoglycemia: insulinautoimmune syndrome.
Anonsense thyrotropin receptor gene mutation RX is associated with congenitalhypothyroidism and heart defects. Prader-Willi syndrome and growth hormone deficiency. Decreased retinal nerve fiber layer thickness in patients with congenital isolated growth hormone deficiency. Corneal properties in children with congenital isolated growth hormone deficiency.
Int J Ophthalmol. Evaluation of asymmetric dimethylarginine ADMA levels in panik yüksek tansiyon with growth hormone deficiency.
Corneal kalp sağlığı klinikleri şikago. characteristics in children with diabetes mellitus. Int Ophthalmol. Diseases accompanying congenital hypothyroidism.
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A girl with steroid cell ovarian tumor misdiagnosed as non-classical congenital adrenal hyperplasia. Increased central corneal thickness in patients with Turner syndrome. A common thyroid peroxidase gene mutation GR in Turkish patients with congenital hypothyroidism could be due to a founder effect. An evaluation of heart rate variability and its modifying factors in children with type 1 diabetes.
Kalp sağlığı klinikleri şikago. Young. Adherence to growth hormone therapy: results of a multicenter study. Endocr Pract. Prevalence and long-term follow-up outcomes of testicular adrenal rest tumours in children andadolescent males with congenital adrenal hyperplasia. Clin Endocrinol Oxf. Evaluation of bone mineral density in children with type 1 diabetes mellitus.
Long-term follow-up of Cushing's disease:a case report.
MR altında hangi durumlarda prostat biyopsisi yapılıyor?
Hyperinsulinemic hypoglycemia: experience in a series of 17 cases. Prevalence of hyperthyrotropinemia in obese children before and after weight loss. Eat Weight Disord. Diabetes mellitus with Laron syndrome: case report.
Report of the first case of precocious puberty in Rett syndrome. Peroxisome proliferator activated receptor PPAR -gamma concentrations in childhood obesity. Scand J Clin Lab Invest. Early subclinical left-ventricular dysfunction in obese nonhypertensive children: a tissue Doppler imaging study. Pediatr Cardiol.