Ben Chehida A[Author] - Search Results

Year	Number of Results
1999	1
2007	1
2008	2
2009	6
2010	1
2011	4
2013	1
2015	6
2016	4
2017	2
2018	5
2019	4
2020	4
2021	1
2024	0

1

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. Ben Abdelaziz R, et al. Among authors: ben chehida a. J Pediatr Endocrinol Metab. 2020 Jul 11:/j/jpem.ahead-of-print/jpem-2020-0025/jpem-2020-0025.xml. doi: 10.1515/jpem-2020-0025. Online ahead of print. J Pediatr Endocrinol Metab. 2020. PMID: 32653876 Review.

2

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. Ben Abdelaziz R, et al. Among authors: ben chehida a. Tunis Med. 2018 Jan;96(1):1-5. Tunis Med. 2018. PMID: 30324984 Free article.

3

Incidence of mucopolysaccharidoses in Tunisia.

Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Ben Chehida A, Chemli J, Monastiri K, Chaabouni M, Sanhagi H, Zouari B, Kaabachi N, Ben Dridi MF. Ben Turkia H, et al. Among authors: ben chehida a. Tunis Med. 2009 Nov;87(11):782-5. Tunis Med. 2009. PMID: 20209839 Free article.

4

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. Ben Abdelaziz R, et al. Among authors: ben chehida a. Arch Pediatr. 2019 Jan;26(1):1-5. doi: 10.1016/j.arcped.2018.10.003. Epub 2018 Dec 13. Arch Pediatr. 2019. PMID: 30554851

5

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome.

Kallabi F, Belghuith N, Aloulou H, Kammoun T, Ghorbel S, Hajji M, Gallas S, Chemli J, Chabchoub I, Azzouz H, Ben Chehida A, Sfaihi L, Makni S, Amouri A, Keskes L, Tebib N, Ben Becher S, Hachicha M, Kamoun H. Kallabi F, et al. Among authors: ben chehida a. Arch Med Res. 2016 Feb;47(2):105-10. doi: 10.1016/j.arcmed.2016.04.004. Epub 2016 Apr 28. Arch Med Res. 2016. PMID: 27133709

6

Renal Involvement in 2 Siblings With Cockayne Syndrome.

Ben Chehida A, Ghali N, Ben Abdelaziz R, Ben Moussa F, Tebib N. Ben Chehida A, et al. Iran J Kidney Dis. 2017 May;11(3):253-255. Iran J Kidney Dis. 2017. PMID: 28575888 Free article.

7

Non-ketotic hyperglycinaemia: a frequent, but poorly diagnosed and managed genetic disorder in Tunisia.

Nasrallah F, Ben Chehida A, Kraoua I, Hadj-Taieb S, Sanhaji H, Tebib N, Feki M, Kaabachi N. Nasrallah F, et al. Among authors: ben chehida a. Arch Dis Child. 2021 Mar;106(3):311. doi: 10.1136/archdischild-2019-318774. Epub 2020 May 13. Arch Dis Child. 2021. PMID: 32404439 No abstract available.

8

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. Ben Abdelaziz R, et al. Among authors: ben chehida a. Tunis Med. 2019 Mar;97(3):426-431. Tunis Med. 2019. PMID: 31729716 Free article.

9

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. Chabchoub I, et al. Among authors: ben chehida a. J Pediatr Hematol Oncol. 2020 May;42(4):310-312. doi: 10.1097/MPH.0000000000001552. J Pediatr Hematol Oncol. 2020. PMID: 31318819

10

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. Ben Abdelaziz R, et al. Among authors: ben chehida a. Eur J Med Genet. 2016 Jan;59(1):16-9. doi: 10.1016/j.ejmg.2015.11.015. Epub 2015 Dec 9. Eur J Med Genet. 2016. PMID: 26691667

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