Halil Saglam
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Explore the profile of Halil Saglam including associated specialties, affiliations and a list of published articles.
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53
Citations
343
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Recent Articles
21.
Atay Z, Yesilkaya E, Savas Erdeve S, Turan S, Akin L, Eren E, et al.
J Clin Endocrinol Metab
. 2016 Mar;
101(5):1980-8.
PMID: 26964727
Aim: The causes of gonadotropin-independent precocious puberty are diverse, and often have overlapping clinical and biochemical features. With the exception of congenital adrenal hyperplasia (CAH), disorders that cause gonadotropin-independent precocious...
22.
Darendeliler F, Yesilkaya E, Bereket A, Bas F, Bundak R, Sari E, et al.
J Clin Res Pediatr Endocrinol
. 2016 Feb;
7(3):183-91.
PMID: 26831551
Objective: Children with Turner syndrome (TS) have a specific growth pattern that is quite different from that of healthy children. Many countries have population-specific growth charts for TS. Considering national...
23.
Erdol S, Saglam H, Basarir T, Okan M
Indian J Pediatr
. 2016 Feb;
83(6):596-7.
PMID: 26830281
No abstract available.
24.
Sari E, Bereket A, Yesilkaya E, Bas F, Bundak R, Aydin B, et al.
Am J Med Genet A
. 2016 Jan;
170A(4):942-8.
PMID: 26788866
To evaluate the anthropometric features of girls with Turner syndrome (TS) at birth and presentation and the effect of karyotype on these parameters. Data were collected from 842 patients with...
25.
Karadag O, Demiroz Abakay C, Ozkan L, Saglam H, Demirkaya M
Turk J Pediatr
. 2015 Dec;
57(2):167-71.
PMID: 26690598
We aimed to evaluate long-term toxicity in children with medulloblastoma treated with postoperative radiotherapy (RT). This study included 21 patients aged 4-16 who had been diagnosed with medulloblastoma. All of...
26.
Cakir E, Saglam H, Eren E, Ozgur T, Tarim O
J Pediatr Endocrinol Metab
. 2015 May;
28(11-12):1219-26.
PMID: 25968434
Objective: The objective of the study was to evaluate the pubertal development and linear growth of Turner Syndrome (TS) girls regularly monitored in our department. Patients And Methods: The data...
27.
Eren E, Saglam H, Caliskan Y, Kiristioglu I, Tarim O
Pediatr Int
. 2015 Apr;
57(5):875-9.
PMID: 25916248
Background: The aim of this retrospective study was to investigate pheochromocytoma (pheo), which is a rare endocrine tumor in the pediatric population. Methods: The medical records of five children with...
28.
Yesilkaya E, Bereket A, Darendeliler F, Bas F, Poyrazoglu S, Aydin B, et al.
J Clin Res Pediatr Endocrinol
. 2015 Mar;
7(1):27-36.
PMID: 25800473
Objective: Turner syndrome (TS) is a chromosomal disorder caused by complete or partial X chromosome monosomy that manifests various clinical features depending on the karyotype and on the genetic background...
29.
Cangul H, Saglam H, Saglam Y, Eren E, Dogan D, Kendall M, et al.
J Pediatr Endocrinol Metab
. 2014 May;
27(9-10):1021-5.
PMID: 24859513
Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and 2% of cases have familial origin. Our aim in this study was to determine the genetic alterations in two...
30.
Cangul H, Schoenmakers N, Saglam H, Doganlar D, Saglam Y, Eren E, et al.
J Pediatr Endocrinol Metab
. 2014 Apr;
27(7-8):731-5.
PMID: 24690939
Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and 2% of cases have a familial origin. Our aim in this study was to determine the genetic alterations in...