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
11.
Erdol S, Karakaya S, Saglam H, Tarim O
Pediatr Dermatol
. 2018 Apr;
35(4):448-452.
PMID: 29635770
Background/objectives: Chromhidrosis is a rare condition of which there are only a few case reports in the literature. The aim of this study was to evaluate clinical, laboratory, and possible...
12.
Erdol S, Saglam H
J Pediatr Endocrinol Metab
. 2018 Apr;
31(4):399-405.
PMID: 29614848
Background: The purpose of this study is to help elucidate which part of the mitochondria is causing a problem through anamnesis, physical examination, and routine biochemical tests in the event...
13.
Cekic S, Saglam H, Gorukmez O, Yakut T, Tarim O, Kilic S
J Clin Immunol
. 2017 Jul;
37(6):524-528.
PMID: 28681255
Purpose: Homozygous mutations in the HAX1 gene cause an autosomal recessive form of severe congenital neutropenia (SCN). There are limited data on cases of gonadal insufficiency that involve the HAX1...
14.
Saglam H, Erdol S, Dorum S
J Clin Res Pediatr Endocrinol
. 2017 Jul;
9(3):229-236.
PMID: 28663156
Objective: Hypophosphatasia (HPP) is a rare, commonly unrecognized hereditary mineralization defect with a dramatically poor prognosis in severe cases. This study is the first to examine the detailed clinical and...
15.
Erdol S, Ture M, Baytan B, Yakut T, Saglam H
J Pediatr Hematol Oncol
. 2016 Oct;
38(8):661-662.
PMID: 27769081
There are published reports stating that some of the congenital metabolic diseases, such as lysinuric protein intolerance, multiple sulphatase deficiency, galactosemia, Gaucher disease, Pearson syndrome, and galactosialidosis, might lead to...
16.
Nicholas A, Serra E, Cangul H, Alyaarubi S, Ullah I, Schoenmakers E, et al.
J Clin Endocrinol Metab
. 2016 Aug;
101(12):4521-4531.
PMID: 27525530
Context: Lower TSH screening cutoffs have doubled the ascertainment of congenital hypothyroidism (CH), particularly cases with a eutopically located gland-in-situ (GIS). Although mutations in known dyshormonogenesis genes or TSHR underlie...
17.
Hatun S, Demirbilek H, Darcan S, Yuksel A, Binay C, Simsek D, et al.
Diabetes Res Clin Pract
. 2016 Jul;
119:32-40.
PMID: 27423071
Aims: To evaluate the management strategies, glycemic control and complications of pediatric type 1 diabetes mellitus (T1DM) patients in Turkey. Methods: Study included 498 patients with T1DM between the ages...
18.
Baric I, Erdol S, Saglam H, Lovric M, Beluzic R, Vugrek O, et al.
JIMD Rep
. 2016 May;
31:101-106.
PMID: 27207470
Glycine N-methyltransferase deficiency is an inherited disorder of methionine metabolism, reported so far in only four patients and characterised by permanent hypermethioninemia. This disorder has been considered as probably benign...
19.
Erdol S, Saglam H
J Clin Res Pediatr Endocrinol
. 2016 Apr;
8(3):330-3.
PMID: 27086477
Objective: Inherited metabolic diseases (IMDs) can affect many organ systems, including the endocrine system. There are limited data regarding endocrine dysfunctions related to IMDs in adults, however, no data exist...
20.
Erdol S, Cekic S, Caki Kilic S, Saglam H, Kilic S
Rheumatol Int
. 2016 Mar;
36(7):1011-3.
PMID: 26965418
No abstract available.