OpenURL Connection Search

Select item for more details and to access through your institution.

H syndrome with histological features of Langerhans cell histiocytosis.
Published in:
2016
By:
- Korbi, Mouna;
- Aounallah, Amina;
- Hmida, Dorra;
- Ghariani, Najet;
- Saidi, Wafa;
- Boussofara, Lobna;
- Belajouza, Colandone;
- Jonard, Laurence;
- Sriha, Badreddine;
- Saad, Ali;
- Denguezli, Mohamed;
- Nouira, Rafiaa
Publication type:
Case Study
Functional analysis of MMR gene VUS from potential Lynch syndrome patients.
Published in:
PLoS ONE, 2024, v. 19, n. 6, p. 1, doi. 10.1371/journal.pone.0304141
By:
- Mahdouani, Marwa;
- Zhuri, Drenushe;
- Sezginer Guler, Hazal;
- Hmida, Dorra;
- Sana, Mokni;
- Azaza, Mohamed;
- Ben Said, Mariem;
- Masmoudi, Saber;
- Hmila, Fahmi;
- Youssef, Sabri;
- Ben Sghaier, Rihab;
- Brieger, Angela;
- Zeuzem, Stefan;
- Saad, Ali;
- Gurkan, Hakan;
- Yalcintepe, Sinem;
- Gribaa, Moez;
- Plotz, Guido
Publication type:
Article
The Contribution of molecular cytogenetics to diagnosis and genetic counseling of microdeletional syndromes in neonatal period.
Published in:
Perinatal Journal, 2024, v. 32, p. 27, doi. 10.59215/prn.24.032supp034
By:
- Barka, Mariem;
- Mghirbi, Oussama;
- Chaieb, Salma;
- Khelifi, Amani;
- Brahem, Donia;
- Taamli, Maha;
- Ghith, Aida;
- Soyed, Nassima;
- Hmida, Dorra;
- Nouri, Sonia;
- Mougou, Soumaya;
- Mahdhaoui, Nabiha
Publication type:
Article
Homozygous mutation in murine retrovirus integration site 1 gene associated with a non‐syndromic form of isolated familial achalasia.
Published in:
Neurogastroenterology & Motility, 2020, v. 32, n. 12, p. 1, doi. 10.1111/nmo.13923
By:
- Koehler, Katrin;
- Hmida, Dorra;
- Schlossmann, Jens;
- Landgraf, Dana;
- Reisch, Nicole;
- Schuelke, Markus;
- Huebner, Angela
Publication type:
Article
Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes.
Published in:
Genetics Research International, 2014, p. 1, doi. 10.1155/2014/210418
By:
- Brahim, Dorra Hmida-Ben;
- Chourabi, Marwa;
- Amor, Sana Ben;
- Harrabi, Imed;
- Trabelsi, Saoussen;
- Haddaji-Mastouri, Marwa;
- Gribaa, Moez;
- Sassi, Sihem;
- Gahbiche, Fatma Ezzahra;
- Lamouchi, Turkia;
- Mougou-Zereli, Soumaya;
- Ammou, Sofiane Ben;
- Saad, Ali
Publication type:
Article
Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer.
Published in:
PLoS ONE, 2022, v. 17, n. 12, p. 1, doi. 10.1371/journal.pone.0278283
By:
- Mahdouani, Marwa;
- Ben Ahmed, Slim;
- Hmila, Fahmi;
- Rais, Henda;
- Ben Sghaier, Rihab;
- Saad, Hanene;
- Ben Said, Mariem;
- Masmoudi, Saber;
- Hmida, Dorra;
- Brieger, Angela;
- Zeuzem, Stefan;
- Saad, Ali;
- Gribaa, Moez;
- Plotz, Guido
Publication type:
Article
UHPLC-APCI-MS Profiling of Triacylglycerols in Vegetable Oils-Application to the Analysis of Four North African Sesame Seed Varieties.
Published in:
Food Analytical Methods, 2017, v. 10, n. 8, p. 2827, doi. 10.1007/s12161-017-0851-0
By:
- Ben Arfa, Kaouther;
- de Person, Marine;
- Hmida, Dorra;
- Bleton, Jean;
- Boukhchina, Sadok;
- Tchapla, Alain;
- Héron, Sylvie;
- Moussa, Fathi
Publication type:
Article

Found: 7

H syndrome with histological features of Langerhans cell histiocytosis.

Functional analysis of MMR gene VUS from potential Lynch syndrome patients.

The Contribution of molecular cytogenetics to diagnosis and genetic counseling of microdeletional syndromes in neonatal period.

Homozygous mutation in murine retrovirus integration site 1 gene associated with a non‐syndromic form of isolated familial achalasia.

Modulation at Age of Onset in Tunisian Huntington Disease Patients: Implication of New Modifier Genes.

Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer.

UHPLC-APCI-MS Profiling of Triacylglycerols in Vegetable Oils-Application to the Analysis of Four North African Sesame Seed Varieties.