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Suggested authors matching "AUTH:Ben Abdelaziz R" with an ORCID

Rim BEN ABDELAZIZ
Faculté de Médecine de Tunis
9
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47
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TTCT 1471 mutation in lysnuric protein intolerance: Clinical features of a Tunisian paediatric series.
Jbebli E, Jbeli Y, Amdouni R, Ben Abdelaziz R, Boudabous H, Ben Chehida A, Abdelmoula S
Tunis Med, 102(5):284-288, 05 May 2024
Cited by: 0 articles | PMID: 38801286 | PMCID: PMC11358835
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Morning specimen is not representative of metabolic control in Tunisian children with phenylketonuria: a repeated cross-sectional study.
Ben Abdelaziz R, Tangour N, Ben Chehida A, Haj Taieb S, Feki M, Azzouz H, Tebib N
J Pediatr Endocrinol Metab, /j/jpem.ahead-of-print/jpem-2020-0025/jpem-2020-00, 11 Jul 2020
Cited by: 0 articles | PMID: 32653876
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Quality of life and associated factors in parents of children with late diagnosed phenylketonuria. A cross sectional study in a developing country (Tunisia).
Ben Abdelaziz R, Ben Chehida A, Kachouri H, Ben Messaoud S, Ferchichi M, Ben Ameur Z, Sassi Y, Abdelmoula MS, Azzouz H, Tebib N
J Pediatr Endocrinol Metab, 33(7):901-913, 01 Jul 2020
Cited by: 3 articles | PMID: 32639944
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Hemophagocytic Lymphohistiocytosis: A Rare Complication of an Ultrarare Lysosomal Storage Disease.
Chabchoub I, Boudabbous H, Maaloul I, Ben Abdelaziz R, Ben Chehida A, Ayadi L, Kamoun T, Tebib N, Boudaouara T, Bekri S, Hachicha M
J Pediatr Hematol Oncol, 42(4):310-312, 01 May 2020
Cited by: 1 article | PMID: 31318819
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Role play for genetic counseling learning: Value and students perceptions.
Ben Abdelaziz R, Boudabous H, Hajji H, Ben Messaoud S, Azzouz H, Ben Chehida A, Tebib N
Tunis Med, 97(3):426-431, 01 Mar 2019
Cited by: 1 article | PMID: 31729716
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High Frequency of Cardiovascular Complications in Tunisian Kawasaki Disease Patients: Need for a Further Awareness.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Boudabous H, Oujra M, Ben Turkia H, Abdelmoula MS, Azzouz H, Hakim K, Tebib N
J Trop Pediatr, 65(3):217-223, 01 Jun 2019
Cited by: 2 articles | PMID: 29982732
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Correction to: Full title: peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study.
Ben Abdelaziz R, Hafsi H, Hajji H, Boudabous H, Ben Chehida A, Mrabet A, Boussetta K, Barsaoui S, Sammoud A, Hamzaoui M, Azzouz H, Tebib N
BMC Pediatr, 18(1):307, 24 Sep 2018
Cited by: 1 article | PMID: 30249232 | PMCID: PMC6154950
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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.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Mansouri H, Boudabous H, Hakim K, Ben Ali N, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Azzouz H, Tebib N
J Pediatr Endocrinol Metab, 31(9):979-986, 01 Sep 2018
Cited by: 6 articles | PMID: 30110253
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Factors predictive of prognosis of infantile spasms. A retrospective study in a low-income country.
Ben Abdelaziz R, Ben Chehida A, Lamouchi M, Ben Messaoud S, Ali Mohamed D, Boudabous H, Abdelmoula MS, Azzouz H, Tebib N
Arch Pediatr, 26(1):1-5, 13 Dec 2018
Cited by: 0 articles | PMID: 30554851
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Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Ben Ali N, Boudabous H, Ben Abdelaziz I, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Fradj M, Azzouz H, Tebib N
Neuropediatrics, 50(1):22-30, 11 Oct 2018
Cited by: 5 articles | PMID: 30308687
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Patient-management Problem (PMP) for paediatrics learning: Value and students perceptions.
Ben Abdelaziz R, Hajji H, Boudabous H, Ben Chehida A, Mrad-Mazigh S, Azzouz H, Tebib N
Tunis Med, 96(1):1-5, 01 Jan 2018
Cited by: 2 articles | PMID: 30324984
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Peripheral venous catheter complications in children: predisposing factors in a multicenter prospective cohort study.
Ben Abdelaziz R, Hafsi H, Hajji H, Boudabous H, Ben Chehida A, Mrabet A, Boussetta K, Barsaoui S, Sammoud A, Hamzaoui M, Azzouz H, Tebib N
BMC Pediatr, 17(1):208, 19 Dec 2017
Cited by: 12 articles | PMID: 29258474 | PMCID: PMC5735659
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Diagnosis of Mediterranean visceral leishmaniasis by detection of Leishmania-related antigen in urine and oral fluid samples.
Ben-Abid M, Galaï Y, Habboul Z, Ben-Abdelaziz R, Ben-Sghaier I, Aoun K, Bouratbine A
Acta Trop, 167:71-72, 22 Dec 2016
Cited by: 5 articles | PMID: 28017861
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Renal Involvement in 2 Siblings With Cockayne Syndrome.
Ben Chehida A, Ghali N, Ben Abdelaziz R, Ben Moussa F, Tebib N
Iran J Kidney Dis, 11(3):253-255, 01 May 2017
Cited by: 4 articles | PMID: 28575888
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A novel homozygous missense mutation in the insulin receptor gene results in an atypical presentation of Rabson-Mendenhall syndrome.
Ben Abdelaziz R, Ben Chehida A, Azzouz H, Boudabbous H, Lascols O, Ben Turkia H, Tebib N
Eur J Med Genet, 59(1):16-19, 09 Dec 2015
Cited by: 6 articles | PMID: 26691667
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[Inborn metabolic disorders in Tunisia: challenges, experience and hopes].
Ben Dridi MF, Ben Turkia H, Azzouz H, Ben Chehida A, Ben Abdelaziz R, Tebib N
Arch Pediatr, 22(5 suppl 1):3-4, 01 May 2015
Cited by: 1 article | PMID: 26112494
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[Renal involvement in glycogen storage disease type 1: Practical issues].
Ben Chehida A, Bensmaïl T, Ben Rehouma F, Ben Abdelaziz R, Azzouz H, Boudabbous H, Slim Abdelmoula M, Abdelhak S, Kaabachi N, Ben Turkia H, Tebib N
Nephrol Ther, 11(4):240-245, 06 May 2015
Cited by: 1 article | PMID: 25957470
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[Rosai -Dorfman disease: a two cases report].
Ben Turkia H, Ben Romdhane M, Azzouz H, Ben Chehida A, Abdelmoula MS, Ben Abdelaziz R, Tebib N, Ben Messoud M, Sahtout S, Chelly I, Zitouni M, Mnif E, Ben Dridi MF
Tunis Med, 89(5):497-501, 01 May 2011
Cited by: 1 article | PMID: 21557191
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