Abdelhadi M Habeb
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Explore the profile of Abdelhadi M Habeb including associated specialties, affiliations and a list of published articles.
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19
Citations
263
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Recent Articles
1.
Habeb A, Deeb A, Elbarbary N, Beshyah S
Diabetes Res Clin Pract
. 2019 Dec;
159:107975.
PMID: 31830516
Aim: To ascertain the awareness and practice of neonatal diabetes mellitus (NDM) among paediatricians in Arab countries. Methods: An online questionnaire was distributed to physicians associated with the Arab Society...
2.
Habeb A, Flanagan S, Zulali M, Abdullah M, Pomahacova R, Boyadzhiev V, et al.
Diabetologia
. 2018 Feb;
61(5):1027-1036.
PMID: 29450569
Aims/hypothesis: Diabetes is one of the cardinal features of thiamine-responsive megaloblastic anaemia (TRMA) syndrome. Current knowledge of this rare monogenic diabetes subtype is limited. We investigated the genotype, phenotype and...
3.
Moran C, Habeb A, Kahaly G, Kampmann C, Hughes M, Marek J, et al.
J Endocr Soc
. 2017 Dec;
1(9):1203-1212.
PMID: 29264576
Resistance to thyroid hormone (RTH) due to homozygous defects is exceptionally rare, with only five kindreds reported worldwide. Cardiac dysfunction, which can be life-threatening, is recognized in the disorder. Here...
4.
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...
5.
Morsy M, Algrigri O, Salem S, Abosedera M, Abutaleb A, Al-Harbi K, et al.
Saudi Med J
. 2016 Jul;
37(7):767-72.
PMID: 27381537
Objectives: To to define the frequency and patterns of congenital heart disease (CHD) among children with Down syndrome (DS) in Northwest Saudi Arabia. Methods: We included children with confirmed DS...
6.
Dimitri P, De Franco E, Habeb A, Gurbuz F, Moussa K, Taha D, et al.
Am J Med Genet A
. 2016 May;
170(7):1918-23.
PMID: 27148679
Neonatal diabetes and hypothyroidism (NDH) syndrome was first described in 2003 in a consanguineous Saudi Arabian family where two out of four siblings were reported to have presented with proportionate...
7.
Ahmed A, Al-Maghamsi M, Al-Harbi A, Eid I, Baghdadi H, Habeb A
J Pediatr Endocrinol Metab
. 2015 Nov;
29(3):259-64.
PMID: 26565539
Background: Raising the awareness of childhood diabetes symptoms can reduce the frequency of diabetic ketoacidosis (DKA) at onset of type 1 diabetes (T1D). However, data on the effectiveness of such...
8.
Habeb A, Deeb A, Johnson M, Abdullah M, Abdulrasoul M, Al-Awneh H, et al.
Horm Res Paediatr
. 2015 Feb;
83(3):190-7.
PMID: 25659842
Background: Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 mutations and characterized by early-onset diabetes and skeletal dysplasia. Hepatic dysfunction has been reported in 60% of patients. Aims: To describe...
9.
Habeb A, Zulali M, Yamani A, Yassine S
Saudi J Kidney Dis Transpl
. 2014 Mar;
25(2):376-80.
PMID: 24626007
Neonatal adrenal hematoma is a rare finding that can be discovered incidentally or presents with various symptoms. However, urinary tract infection (UTI) has not been reported in association with this...
10.
Habeb A
Libyan J Med
. 2013 Jun;
8(1):21137.
PMID: 23759358
Background: Wolcott-Rallison syndrome (WRS) is caused by recessive EIF2AK3 gene mutations and characterized by permanent neonatal diabetes (PNDM), skeletal dysplasia, and recurrent hepatitis. The frequency of this rare syndrome is...