E-LIB Suche - Ergebnisse für: Abidi, Kamel

1

HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tun..:

M'dimegh, Saoussen ; Aquaviva-bourdain, Cécile ; Omezzine, Asma...
Journal of Clinical Laboratory Analysis. 31 (2016) 3 - p. e22053 , 2016

Link: https://doi.org/10.1002/..

2

A novel mutation in the AGXT gene causing primary hyperoxal..:

M'DIMEGH, SAOUSSEN ; AQUAVIVA-BOURDAIN, CÉCILE ; OMEZZINE, ASMA...
Journal of Genetics. 95 (2016) 3 - p. 659-666 , 2016

Link: https://doi.org/10.1007/..

3

Persistance de la veine cave supérieure gauche: à propos d'..:

Abidi, Kamel ; Jellouli, Manel ; Hammi, Yousra.
Pan African Medical Journal. 22 (2015) - p. , 2015

Link: https://doi.org/10.11604..

4

Particularité de la cystinose infantile chez l'enfant tunis..:

Jellouli, Manel ; Turkia, Hadhami Ben ; Abidi, Kamel..
Pan African Medical Journal. 22 (2015) - p. , 2015

Link: https://doi.org/10.11604..

5

Caractéristiques bactériologiques des infections de liquide..:

Jellouli, Manel ; Ferjani, Meriem ; Abidi, Kamel...
Pan African Medical Journal. 22 (2015) - p. , 2015

Link: https://doi.org/10.11604..

6

Tuberculosis following kidney transplantation: report of pa..:

Abidi, Kamel ; Jellouli, Manel ; Hammi, Yousra.
Pan African Medical Journal. 22 (2015) - p. , 2015

Link: https://doi.org/10.11604..

7

Williams-Beuren syndrome associated with single kidney and ..:

Abidi, Kamel ; Jellouli, Manel ; Rabeh, Rania Ben..
Pan African Medical Journal. 22 (2015) - p. , 2015

Link: https://doi.org/10.11604..

8

Maladie cœliaque associée à une maladie de Basedow et un dé..:

Jellouli, Manel ; Abidi, Kamel ; Hammi, Yousra...
Pan African Medical Journal. 22 (2015) - p. , 2015

Link: https://doi.org/10.11604..

9

Detection of a novel splicing mutation causing analbuminemi..:

Bibi, Amina ; Jouini, Latifa ; Sahli, Chaima Abdelhafidh...
Clinical Biochemistry. 45 (2012) 15 - p. 1183-1186 , 2012

Link: https://doi.org/10.1016/..

10

Infantile Parotid Hemangioma With Diagnostic Dilemma: A Cas..:

Abidi, Kamel T ; Kamal, Naglaa M ; Althobaiti, Khaled A...
Clinical Medicine Insights: Case Reports. 15 (2022) - p. 117954762110733 , 2022

Link: https://doi.org/10.1177/..

11

Sjogren–Larsson Syndrome: A case series of five members fro..:

Abidi, Kamel T. ; Kamal, Naglaa M. ; Bakkar A., Ayman A....
Molecular Genetics & Genomic Medicine. 8 (2020) 11 - p. , 2020

Link: https://doi.org/10.1002/..

12

HOGA1 Gene Mutations of Primary Hyperoxaluria Type 3 in Tun..:

M'dimegh, Saoussen ; Aquaviva‐bourdain, Cécile ; Omezzine, Asma...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6817302/. , 2016

Link: http://www.ncbi.nlm.nih...

13

Infantile Parotid Hemangioma With Diagnostic Dilemma: A Cas..:

Abidi, Kamel T ; Kamal, Naglaa M ; Althobaiti, Khaled A...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793416/. , 2022

Link: http://www.ncbi.nlm.nih...

14

Persistent Hypertransaminasemia Uncovered Occult Limb-Girdl..:

Naglaa M. Kamal ; Hamed A. Alghamdi ; Abdulrahman Halabi...
http://jpedres.org/archives/archive-detail/article-preview/persistent-hypertransaminasemia-uncovered-occult-l/16898. , 2018

Link: https://doi.org/10.4274/..

15

Infantile cystinosis: From dialysis to renal transplantatio:

Manel Jellouli ; Meriem Ferjani ; Kamel Abidi...
http://www.sjkdt.org/article.asp?issn=1319-2442;year=2017;volume=28;issue=5;spage=1180;epage=1183;aulast=Jellouli. , 2017

Link: https://doi.org/10.4103/..