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Amel Ben Chehida
Observed names:
A Ben Chehida,
A. Ben Chehida,
Amel Ben-chehida,
Amel Chehida,
Amel ben Chehida,
Ben Chehida, Amel
show all 6
Institutions:
Tunis University,
Hôpital La Rabta,
Faculté de médecine de Tunis,
Tunis El Manar University
Observed institutions:
Tunis University,
Hôpital La Rabta,
Hôpital Mongi Slim,
Military Hospital of Tunis,
Faculté de médecine de Tunis,
Tunis El Manar University
show all 6
ORCID:
0000-0001-7880-3215
Observed ORCID:
0000-0001-7880-3215
OpenAlex ID:
A5081215852
Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
2017
·
Rim Ben Abdelaziz
, Habiba Hafsi
, et al.
·
BMC Pediatrics
·
118
PDF
Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome
2016
·
Fakhri Kallabi
, Neila Belghuith
, et al.
·
Archives of Medical Research
·
32
A Founder Effect of c.257 + 2T > C Mutation in NCF2 Gene Underlies Severe Chronic Granulomatous Disease in Eleven Patients
2016
·
Khaoula Ben-Farhat
, Imen Ben-Mustapha
, et al.
·
Journal of Clinical Immunology
·
18
A novel homozygous missense mutation in the insulin receptor gene results in an atypical presentation of Rabson-Mendenhall syndrome
2015
·
Rim Ben Abdelaziz
, Amel Ben Chehida
, et al.
·
European Journal of Medical Genetics
·
17
Phenotypic continuum of type 2 Gaucher's disease: an intermediate phenotype between perinatal-lethal and classic type 2 Gaucher's disease
2009
·
H Ben Turkia
, N Tebib
, et al.
·
Journal of Perinatology
·
16
Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype
2024
·
Thomas B. Smith
, Robert Kopajtich
, et al.
·
The American Journal of Human Genetics
·
15
Mutation spectrum of glycogen storage disease type Ia in Tunisia: Implication for molecular diagnosis
2007
·
E. Barkaoui
, W. Cherif
, et al.
·
Journal of Inherited Metabolic Disease
·
15
Splicing defects in ABCD1 gene leading to both exon skipping and partial intron retention in X-linked adrenoleukodystrophy Tunisian patient
2015
·
Fakhri Kallabi
, Ikhlass Hadj Salem
, et al.
·
Neuroscience Research
·
12
Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients
2018
·
Sana Ben Messaoud
, Rim Ben Abdelaziz
, et al.
·
Neuropediatrics
·
11
A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients
2018
·
Amel Ben Chehida
, Sana Ben Messaoud
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
11
Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients
2020
·
Fahmi Nasrallah
, Sameh Hadj-Taieb
, et al.
·
Neuropediatrics
·
8
Renal Involvement in 2 Siblings With Cockayne Syndrome.
2017
·
Amel Ben Chehida
, Narjess Ghali
, et al.
·
Iranian Journal of Kidney Diseases
·
8
PDF
First Report of a Molecular Prenatal Diagnosis in a Tunisian Family with Lysinuric Protein Intolerance
2011
·
Nadia Esseghir
, Chiraz Souissi Bouchlaka
, et al.
·
JIMD Reports
·
8
Lipodystrophie congénitale généralisée de type 1 avec atteinte neurologique
2008
·
H. Ben Turkia
, N. Tebib
, et al.
·
Archives de Pédiatrie
·
8
Quality of life and associated factors in parents of children with late diagnosed phenylketonuria. A cross sectional study in a developing country (Tunisia)
2020
·
Rim Ben Abdelaziz
, Amel Ben Chehida
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
7
Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study
2018
·
Rim Ben Abdelaziz
, Habiba Hafsi
, et al.
·
BMC Pediatrics
·
7
PDF
High Frequency of Cardiovascular Complications in Tunisian Kawasaki Disease Patients: Need for a Further Awareness
2018
·
Amel Ben Chehida
, Sana Ben Messaoud
, et al.
·
Journal of Tropical Pediatrics
·
7
Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III
2013
·
Faten Ben Rhouma
, Hatem Azzouz
, et al.
·
Molecular Biology Reports
·
7
Cholestase néonatale révélatrice d’un phénotype intermédiaire d’une maladie de Gaucher type 2
2009
·
H. Ben Turkia
, N. Tebib
, et al.
·
Archives de Pédiatrie
·
7
Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease
2019
·
Imen Chabchoub
, Hela Boudabbous
, et al.
·
Journal of Pediatric Hematology/Oncology
·
6
Self-Reported Anxiety, Depression and Coping in Parents of Children with Phenylketonuria
2019
·
Rim Ben Abdelaziz
, Amel Ben Chehida
, et al.
·
Journal of Developmental and Physical Disabilities
·
6
Complications rénales dans la glycogénose de type 1 : quelles implications pratiques ?
2015
·
Amel Ben Chehida
, Takoua Bensmaïl
, et al.
·
Néphrologie & Thérapeutique
·
6
Glycogen storage disease type I in Tunisia: An epidemiological analysis
2008
·
A. Ben Chehida
, N. Tebib
, et al.
·
Journal of Inherited Metabolic Disease
·
6
Morning specimen is not representative of metabolic control in Tunisian children with phenylketonuria: a repeated cross-sectional study
2020
·
Rim Ben Abdelaziz
, Nizar Tangour
, et al.
·
Journal of Pediatric Endocrinology and Metabolism
·
5
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide withRAF1S259Y neomutation
2019
·
Hager Jaouadi
, Amel Ben Chehida
, et al.
·
Genetics Research
·
5
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Works count:
84
Citation count:
405
H-index:
10
I10-index:
10
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