E-LIB Suche - Ergebnisse für: Azzouz, Haifa

1

Neuroendocrine differentiation in basal cell carcinoma:

Houcine, Yoldez ; Chelly, Ines ; Zehani, Alia...
Journal of Immunoassay and Immunochemistry. 38 (2017) 5 - p. 487-493 , 2017

Link: https://doi.org/10.1080/..

2

When trichoscopy enlightens clinics:

Souissi, Asmahen ; Ben Tanfous, Azima ; Azzouz, Haifa...
International Journal of Dermatology. 55 (2016) 11 - p. 1278-1280 , 2016

Link: https://doi.org/10.1111/..

3

A case of primary malignant fibrous histiocytoma of the duo..:

Makni, Amin ; Chebbi, Faouzi ; Azzouz, Haifa...
International Journal of Surgery Case Reports. 2 (2011) 6 - p. 103-105 , 2011

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

4

Subcutis calcinosis caused by injection of calcium-containi..:

Lilia Ben Fatma ; Zohra El Ati ; Haifa Azzouz...
http://www.sjkdt.org/article.asp?issn=1319-2442;year=2014;volume=25;issue=5;spage=1068;epage=1071;aulast=Fatma. , 2014

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

5

Kaposi′s sarcoma with HHV8 infection and ANCA-associated va..:

Lilia Ben Fatma ; Lamia Rais ; Amel Mebazza...
http://www.sjkdt.org/article.asp?issn=1319-2442;year=2013;volume=24;issue=6;spage=1199;epage=1202;aulast=Fatma. , 2013

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

6

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
Genes. 13 (2022) 8 - p. 1355 , 2022

Link: https://doi.org/10.3390/..

7

Identification of novel pathogenic MSH2 mutation and new DN..:

Jaballah-Gabteni, Amira ; Tounsi, Haifa ; Kabbage, Maria...
Journal of Translational Medicine. 17 (2019) 1 - p. , 2019

Link: https://doi.org/10.1186/..

8

CDH1 Germline Variants in a Tunisian Cohort with Hereditary..:

Ben Aissa-Haj, Jihenne ; Kabbage, Maria ; Othmen, Houcemeddine...
Genes. 13 (2022) 3 - p. 400 , 2022

Link: https://doi.org/10.3390/..

9

Identification of novel pathogenic MSH2 mutation and new DN..:

Jaballah-Gabteni, Amira ; Tounsi, Haifa ; Kabbage, Maria...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12967-019-1961-9. , 2019

Link: https://hal-riip.archive..

10

Identification of novel pathogenic MSH2 mutation and new DN..:

Jaballah-Gabteni, Amira ; Tounsi, Haifa ; Kabbage, Maria...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12967-019-1961-9. , 2019

Link: https://riip.hal.science..

11

Identification of novel pathogenic MSH2 mutation and new DN..:

Jaballah-Gabteni, Amira ; Tounsi, Haifa ; Kabbage, Maria...
info:eu-repo/semantics/altIdentifier/doi/10.1186/s12967-019-1961-9. , 2019

Link: https://hal-riip.archive..

12

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9407052/. , 2022

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

13

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes13081355. , 2022

Link: https://hal-amu.archives..

14

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Kabbage, Maria ; Ben Aissa-Haj, Jihenne ; Othman, Houcemeddine...
info:eu-repo/semantics/altIdentifier/doi/10.3390/genes13081355. , 2022

Link: https://amu.hal.science/..

15

A Rare MSH2 Variant as a Candidate Marker for Lynch Syndrom..:

Maria Kabbage ; Jihenne Ben Aissa-Haj ; Houcemeddine Othman...
Molecular Genetics and Genomics. , 2022

Link: https://doi.org/10.3390/..