Tal Almagor
Overview
Explore the profile of Tal Almagor including associated specialties, affiliations and a list of published articles.
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Articles
9
Citations
32
Followers
0
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Recent Articles
1.
Levshtein A, Sharkia M, Shimshi-Barash M, Almagor T, Albertsson-Wikland K, Hochberg Z, et al.
Front Endocrinol (Lausanne)
. 2025 Mar;
16:1483199.
PMID: 40034226
Context: Physiological growth hormone is secreted during slow-wave sleep. Traditionally, growth hormone (GH) therapy is given in daily GH injections before sleep. While morning and evening GH injections produce comparable...
2.
Abu Hanna F, Sirkin M, Ilovich B, Egbarieh R, Tatour S, Lahad A, et al.
Eur J Pediatr
. 2025 Feb;
184(3):199.
PMID: 39948300
Conclusion: Effective management of celiac disease, including timely TTG normalization and sustained lower TTG levels, may be important for reducing the risk of subsequent development of ADs in pediatric-onset CeD....
3.
Almagor T, Almashanu S, Elias-Assad G, Admoni O, Ludar H, London S, et al.
Endocr Connect
. 2024 Oct;
13(12).
PMID: 39413214
Objectives: The incidence of congenital hypothyroidism (CH) has increased worldwide over the last decades, mainly due to the lowering of screening thresholds, resulting in the increased identification of newborns with...
4.
Almagor T, Rath S, Nachtigal D, Sharroni Z, Elias-Assad G, Hess O, et al.
Eur Thyroid J
. 2021 Jun;
10(3):215-221.
PMID: 34178707
Background: An association between hearing impairment (HI) and congenital hypothyroidism (CH) has been reported previously. However, in general, studies were retrospective and had small sample sizes, and the results were...
5.
Tenenbaum-Rakover Y, Admoni O, Elias-Assad G, London S, Noufi-Barhoum M, Ludar H, et al.
Endocr Connect
. 2021 May;
10(6):620-629.
PMID: 34009138
Objective: Disorders of sex development (DSD) are defined as congenital conditions in which the development of chromosomal, gonadal and anatomical sex is atypical. Despite wide laboratory and imaging investigations, the...
6.
Curelaru S, Zehavi Y, Almagor T, Spiegel R
Mol Genet Metab Rep
. 2021 Mar;
27:100739.
PMID: 33732620
Niemann-Pick disease Type C (NPC) is a rare autosomal recessive neurovisceral lysosomal disorder. Perinatal and early infantile onset NPC are the most severe types of the disease. Early infantile type...
7.
Admoni O, Rath S, Almagor T, Elias-Assad G, Tenenbaum-Rakover Y
Front Endocrinol (Lausanne)
. 2020 Jun;
11:309.
PMID: 32582023
Autoimmune thyroiditis (AIT) is the most common cause of acquired hypothyroidism in children. The natural outcome of AIT in childhood has been reported previously however follow-up duration is generally short...
8.
Rinawi F, Assa A, Almagor T, Ziv-Baran T, Shamir R
Digestion
. 2019 Sep;
101(6):674-682.
PMID: 31522182
Background And Aims: Growth impairment is common in children with inflammatory bowel diseases (IBD). However, the magnitude of short stature at adulthood is not well characterized. We aimed to determine...
9.
Almagor T, Eisen J, Harris M, Levental-Roberts M, Hess O, Schwartz N, et al.
Harefuah
. 2016 Jan;
154(10):620-3, 677.
PMID: 26742222
Background: Childhood and adolescent obesity is an ongoing problem in the Western World and has increased dramatically over the last four decades. Similar trends have been observed in Israel, but...
10.
Hess O, Admoni O, Khayat M, Elias G, Almagor T, Shalev S, et al.
J Pediatr Endocrinol Metab
. 2012 Aug;
25(5-6):537-40.
PMID: 22876551
Context And Objective: Ghrelin and its receptor, growth hormone secretagogue receptor (GHSR), have key roles in appetite control and growth regulation. To date, only few mutations of GHSR have been...