Autoinflammatory diseases: what is behind them and what is new?

por Maalouly, Michele, Saade, Serena, Kurban, Mazen
Publicado 2022

Plasmacytoid dendritic cells and type I interferons in flares of systemic lupus erythematosus triggered by COVID-19

por Nasser, Nourhane, Kurban, Mazen, Abbas, Ossama
Publicado 2021

Possible Role for Plasmacytoid Dendritic Cells in Pemphigus

por Ramadan, Nehmat, Kurban, Mazen, Abbas, Ossama
Publicado 2019

Scabies in the age of increasing drug resistance

por Khalil, Samar, Abbas, Ossama, Kibbi, Abdul Ghani, Kurban, Mazen
Publicado 2017

Plasmacytoid Dendritic Cells in Pityriasis Rubra Pilaris

por Al-Hage, Jana, Akel, Randa, Kurban, Mazen, Abbas, Ossama
Publicado 2019

Trps1 and Its Target Gene Sox9 Regulate Epithelial Proliferation in the Developing Hair Follicle and Are Associated with Hypertrichosis

por Fantauzzo, Katherine A., Kurban, Mazen, Levy, Brynn, Christiano, Angela M.
Publicado 2012

A novel mutation in the HPGD gene results in the unusual phenotype of palmoplantar keratoderma with digital clubbing and hyperhidrosis

por Stephan, Carla, Hanna, Edith, Nemer, Georges, Abbas, Ossama, Kurban, Mazen
Publicado 2018

A novel pathogenic CDH3 variant underlying heredity hypotrichosis simplex detected by whole-exome sequencing (WES)—a case report

por Kadhi, Ayat, Hamie, Lamiaa, Tamer, Christel, Nemer, Georges, Kurban, Mazen
Publicado 2022

A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance

por Kurban, Mazen, Wajid, Muhammad, Petukhova, Lynn, Shimomura, Yutaka, Christiano, Angela M
Publicado 2011

A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases

por Khalil, Athar, Tanos, Rachel, El-Hachem, Nehmé, Kurban, Mazen, Bouvagnet, Patrice, Bitar, Fadi, Nemer, Georges
Publicado 2017

Genetics of inherited cardiocutaneous syndromes: a review

por Bardawil, Tara, Khalil, Samar, Bergqvist, Christina, Abbas, Ossama, Kibbi, Abdul Ghani, Bitar, Fadi, Nemer, Georges, Kurban, Mazen
Publicado 2016

A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations

por Khalil, Athar, Al-Haddad, Christiane, Hariri, Hadla, Shibbani, Kamel, Bitar, Fadi, Kurban, Mazen, Nemer, Georges, Arabi, Mariam
Publicado 2017

Prevalence of Human Papillomavirus (HPV)-16 in Different Dental Infections in the Lebanese Population

por Khalil, Wael, Alaa El Din, Ferdos, Jaffal, Marwa, Kanj, Abd El Hadi, Nabbouh, Ali, Kurban, Mazen, Rahal, Elias A, Matar, Ghassan M
Publicado 2023

Identification of Several Mutations in ATP2C1 in Lebanese Families: Insight into the Pathogenesis of Hailey-Hailey Disease

por Btadini, Waed, Abou Hassan, Ossama K., Saadeh, Dana, Abbas, Ossama, Ballout, Farah, Kibbi, Abdul-Ghani, Dbaibo, Ghassan, Darwiche, Nadine, Nemer, Georges, Kurban, Mazen
Publicado 2015

Integrative Transcriptome Analyses Empower the Anti-COVID-19 Drug Arsenal

por El-Hachem, Nehme, Eid, Edward, Nemer, Georges, Dbaibo, Ghassan, Abbas, Ossama, Rubeiz, Nelly, Zeineldine, Salah, Matar, Ghassan M., Bikorimana, Jean-Pierre, Shammaa, Riam, Haibe-Kains, Benjamin, Kurban, Mazen, Rafei, Moutih
Publicado 2020

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

por Kamar, Amina, Fahed, Akl C., Shibbani, Kamel, El-Hachem, Nehme, Bou-Slaiman, Salim, Arabi, Mariam, Kurban, Mazen, Seidman, Jonathan G., Seidman, Christine E., Haidar, Rachid, Baydoun, Elias, Nemer, Georges, Bitar, Fadi
Publicado 2017

Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth

por DeStefano, Gina M., Kurban, Mazen, Anyane-Yeboa, Kwame, Dall'Armi, Claudia, Di Paolo, Gilbert, Feenstra, Heather, Silverberg, Nanette, Rohena, Luis, López-Cepeda, Larissa D., Jobanputra, Vaidehi, Fantauzzo, Katherine A., Kiuru, Maija, Tadin-Strapps, Marija, Sobrino, Antonio, Vitebsky, Anna, Warburton, Dorothy, Levy, Brynn, Salas-Alanis, Julio C., Christiano, Angela M.
Publicado 2014