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Search Results - Ennouri, Mariem
Search Results - Ennouri, Mariem
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Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations
by
Hotz, Alrun
,
Fölster-Holst, Regina
,
Oji, Vinzenz
,
Bourrat, Emmanuelle
,
Frank, Jorge
,
Marrakchi, Slaheddine
,
Ennouri, Mariem
,
Wankner, Lotta
,
Komlosi, Katalin
,
Alter, Svenja
,
Fischer, Judith
Published in
Genes
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Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype-phenotype correlation
by
Ennouri, Mariem
,
Zimmer, Andreas D
,
Bahloul, Emna
,
Chaabouni, Rim
,
Marrakchi, Slaheddine
,
Turki, Hamida
,
Fakhfakh, Faiza
,
Bougacha-Elleuch, Noura
,
Fischer, Judith
Published in
BMC medical genomics
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Identification of a novel missense mutation in NIPAL4 gene: First 3D model construction predicted its pathogenicity
by
Laadhar, Sahar
,
Ben Mansour, Riadh
,
Marrakchi, Slaheddine
,
Miled, Nabil
,
Ennouri, Mariem
,
Fischer, Judith
,
Kaddechi, Mohamed Ali
,
Turki, Hamida
,
Fakhfakh, Faiza
Published in
Molecular genetics & genomic medicine
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Pustular psoriasis of pregnancy: Clinical and genetic characteristics in a series of eight patients and review of the literature
by
Ennouri, Mariem
,
Bahloul, Emna
,
Sellami, Khadija
,
Marrakchi, Slaheddine
,
Fakhfakh, Faiza
,
Turki, Hamida
,
Bougacha‐Elleuch, Noura
Published in
Dermatologic therapy
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Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying IABCA12/I Mutations
by
Hotz, Alrun
,
Fölster-Holst, Regina
,
Oji, Vinzenz
,
Bourrat, Emmanuelle
,
Frank, Jorge
,
Marrakchi, Slaheddine
,
Ennouri, Mariem
,
Wankner, Lotta
,
Komlosi, Katalin
,
Alter, Svenja
,
Fischer, Judith
Published in
Genes
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Pustular Psoriasis of Pregnancy: Clinical and Genetic Characteristics in a Series of 8 Patients and Review of the Literature
by
Mariem, Ennouri
,
Emna, Bahloul
,
Khadija, Sellami
,
Slaheddine, Marrakchi
,
Faiza, Fakhfakh
,
Hamida, Turki
,
Noura, Bougacha-Elleuch
Published in
Dermatologic therapy
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Epidemiological characteristics, management, and outcomes of atrial fibrillation in TUNISIA: Results from the National Tunisian Registry of Atrial Fibrillation (NATURE‐AF)
by
Ouali, Sana
,
Ben Halima, Afef
,
Chabrak, Sonia
,
Chettaoui, Rafik
,
Ben Halima, Manel
,
Haggui, Abdeddayem
,
Krichane, Salma
,
Noureddine, Larbi
,
Marrakchi, Sonia
,
Charfeddine, Selma
,
Hassine, Majed
,
Sayahi, Khaled
,
Abbes Mohamed, Fehmi
,
Nasraoui, Wided
,
Ajmi, Hassen
,
Ben Miled, Mehdi
,
Jebbari, Zeynab
,
Meghaieth, Mohamed Ali
,
Allouche, Emna
,
Mechmeche, Rachid
,
Zakhama, Lilia
,
Sdiri, Wissem
,
Ben Khalfallah, Ali
,
Gharbi, Anissa
,
Milouchi, Sami
,
Neji, Ali
,
Antit, Saoussen
,
Battikh, Kais
,
Drissa, Meriem
,
Kaabachi, Samira
,
Najar, Tarek
,
Tlili, Rami
,
Chahbani, Iheb
,
Charfeddine, Hanene
,
Ben, Mbarek Mohamed
,
Braham, Sami
,
Maatouk, Faouzi
,
Abdesselem, Salem
,
Ayari, Mokdad
,
Garbaa, Riadh
,
Hamrouni, Nabil
,
Mbarek, Dorra
,
Rekik, Hajer
,
Zaghdoudi, Hamda
,
Ayadi, Wacef
,
Baraket, Feriel
,
Ben Brahim, Karim
,
Ben Romdhane, Mariem
,
Bousadia, Habib
,
Brahim, Wassim
,
Mezri, Malek
,
Guesmi, Ali
,
Ounissi, Taha
,
Kammoun, Sofiene
,
Smati, Wajih
,
Tlili, Samir
,
Zoughi, Karim
,
Zemni, Jawher
,
Cheikh Bouhlel, Mahmoud
,
Islem, Sanaa
,
Jemli, Rym
,
Joulak, Anissa
,
Mzoughi, Khadija
,
Naanea, Hela
,
Hached, Leila
,
Hadrich, Moufid
,
Hmem, Mohamed
,
Kacem, Slim
,
Kammoun, Ikram
,
Othmani, Rawdha
,
Ouerghi, Amel
,
Abid, Syrine
,
Ennouri, Ridha
,
Haidar, Sandrine
,
Heraiech, Sihem
,
Jammali, Monia
,
Jarrar, Mourad
,
Riahi, Leila
,
Trimech, Basma
,
Azaiez, Med Ali
,
Azzouzi, Foued
,
Ben Jemaa, Khaled
,
Ben Rejab, Oussema
,
Chrigui, Rim
,
Wechtati, Wejdene
,
Boughzela, Essia
,
Jridi, Gouider
,
Bezdah, Leila
,
Kraiem, Sondes
,
Drissa, Habiba
,
Ben Youssef, Soraya
,
Fehri, Wafa
,
Kachboura, Salem
,
Gamra, Habib
,
Kammoun, Samir
,
Mourali, Mohamed Sami
,
Addad, Faouzi
,
Abid, Leila
Published in
Clinical cardiology (Mahwah, N.J.)
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Long-term clinical follow-up and molecular testing for diagnosis of the first Tunisian family with Alström syndrome
by
Chakroun, Amine
,
Ben Said, Mariem
,
Ennouri, Amine
,
Achour, Imen
,
Mnif, Mouna
,
Abid, Mohamed
,
Ghorbel, Abdelmonem
,
Marshall, Jan D
,
Naggert, Jürgen K
,
Masmoudi, Saber
Published in
European journal of medical genetics
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