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A novel [electronic resource] by
- Arousse, Aycha
- Boussofara, Lobna
- H'mida-Ben Brahim, Dorra
- Migaud, Mélanie
- Aounallah, Amina
- Ghariani, Najet
- Casanova, Jean-Laurent
- Nouira, Rafiaa
- Puel, Anne
- Denguezli, Mohamed
Publication details: JAAD case reports Jul 2018
In:
JAAD case reports vol. 4
Availability: No items available.
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Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor. [electronic resource] by
- H'mida Ben-Brahim, Dorra
- Hammami, Sabeur
- Haddaji Mastouri, Marwa
- Trabelsi, Saoussen
- Chourabi, Maroua
- Sassi, Sihem
- Mougou, Soumaya
- Gribaa, Moez
- Zakhama, Abdelfattah
- Guédiche, Mohamed Neji
- Saad, Ali
Producer: 20160303
In:
Applied & translational genomics vol. 4
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Transient neonatal diabetes mellitus and hypomethylation at additional imprinted loci: novel ZFP57 mutation and review on the literature. [electronic resource] by
- Touati, Ameni
- Errea-Dorronsoro, Javier
- Nouri, Sonia
- Halleb, Yosra
- Pereda, Arrate
- Mahdhaoui, Nabiha
- Ghith, Aida
- Saad, Ali
- Perez de Nanclares, Guiomar
- H'mida Ben Brahim, Dorra
Producer: 20190415
In:
Acta diabetologica vol. 56
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Amelanotic melanoma arising in an area of SLURP-1 mutated Mal de Meleda. [electronic resource] by
- Arousse, Aycha
- Mokni, Sana
- H'mida Ben Brahim, Dorra
- Bdioui, Ahlem
- Aounallah, Amina
- Gammoudi, Rima
- Saidi, Wafa
- Boussofara, Lobna
- Ghariani, Najet
- Denguezli, Mohamed
- Belajouza, Colandane
- Nouira, Rafia
Producer: 20191125
In:
International journal of dermatology vol. 58
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Rundataxin, a novel protein with RUN and diacylglycerol binding domains, is mutant in a new recessive ataxia. [electronic resource] by
- Assoum, Mirna
- Salih, Mustafa A
- Drouot, Nathalie
- H'Mida-Ben Brahim, Dorra
- Lagier-Tourenne, Clotilde
- AlDrees, Abdulmajeed
- Elmalik, Salah A
- Ahmed, Taha S
- Seidahmed, Mohammad Z
- Kabiraj, Mohammad M
- Koenig, Michel
Producer: 20101007
In:
Brain : a journal of neurology vol. 133
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Assessment of MYCN amplification status in Tunisian neuroblastoma: CISH and MLPA combining approach. [electronic resource] by
- H'Mida Ben Brahim, Dorra
- Trabelsi, Saoussen
- Chabchoub, Imen
- Gargouri, Inesse
- Harrabi, Imed
- Moussa, Adnene
- Chourabi, Maroua
- Haddaji, Marwa
- Sassi, Sihem
- Mougou, Soumaya
- Gribaa, Moez
- Ben Ahmed, Slim
- Zakhama, Abdelfattah
- Nouri, Abdellatif
- Saad, Ali
Producer: 20160301
In:
La Tunisie medicale vol. 93
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Molecular Diagnostic and Prognostic Subtyping of Gliomas in Tunisian Population. [electronic resource] by
- Trabelsi, Saoussen
- Chabchoub, Imen
- Ksira, Iadh
- Karmeni, Nadhir
- Mama, Nadia
- Kanoun, Samia
- Burford, Anna
- Jury, Alexa
- Mackay, Alan
- Popov, Sergey
- Bouaouina, Noureddine
- Ben Ahmed, Slim
- Mokni, Moncef
- Tlili, Kalthoum
- Krifa, Hedi
- Yacoubi, Mohamed Tahar
- Jones, Chris
- Saad, Ali
- H'mida Ben Brahim, Dorra
Producer: 20170630
In:
Molecular neurobiology vol. 54
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Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolism. [electronic resource] by
- Fiskerstrand, Torunn
- H'mida-Ben Brahim, Dorra
- Johansson, Stefan
- M'zahem, Abderrahim
- Haukanes, Bjørn Ivar
- Drouot, Nathalie
- Zimmermann, Julian
- Cole, Andrew J
- Vedeler, Christian
- Bredrup, Cecilie
- Assoum, Mirna
- Tazir, Meriem
- Klockgether, Thomas
- Hamri, Abdelmadjid
- Steen, Vidar M
- Boman, Helge
- Bindoff, Laurence A
- Koenig, Michel
- Knappskog, Per M
Producer: 20101007
In:
American journal of human genetics vol. 87
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ENPP1 Mutation Causes Recessive Cole Disease by Altering Melanogenesis. [electronic resource] by
- Chourabi, Marwa
- Liew, Mei Shan
- Lim, Shawn
- H'mida-Ben Brahim, Dorra
- Boussofara, Lobna
- Dai, Liang
- Wong, Pui Mun
- Foo, Jia Nee
- Sriha, Badreddine
- Robinson, Kim Samirah
- Denil, Simon
- Common, John Ea
- Mamaï, Ons
- Ben Khalifa, Youcef
- Bollen, Mathieu
- Liu, Jianjun
- Denguezli, Mohamed
- Bonnard, Carine
- Saad, Ali
- Reversade, Bruno
Producer: 20190307
In:
The Journal of investigative dermatology vol. 138
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Functional diversity and cooperativity between subclonal populations of pediatric glioblastoma and diffuse intrinsic pontine glioma cells. [electronic resource] by
- Vinci, Mara
- Burford, Anna
- Molinari, Valeria
- Kessler, Ketty
- Popov, Sergey
- Clarke, Matthew
- Taylor, Kathryn R
- Pemberton, Helen N
- Lord, Christopher J
- Gutteridge, Alice
- Forshew, Tim
- Carvalho, Diana
- Marshall, Lynley V
- Qin, Elizabeth Y
- Ingram, Wendy J
- Moore, Andrew S
- Ng, Ho-Keung
- Trabelsi, Saoussen
- H'mida-Ben Brahim, Dorra
- Entz-Werle, Natacha
- Zacharoulis, Stergios
- Vaidya, Sucheta
- Mandeville, Henry C
- Bridges, Leslie R
- Martin, Andrew J
- Al-Sarraj, Safa
- Chandler, Christopher
- Sunol, Mariona
- Mora, Jaume
- de Torres, Carmen
- Cruz, Ofelia
- Carcaboso, Angel M
- Monje, Michelle
- Mackay, Alan
- Jones, Chris
Producer: 20190510
In:
Nature medicine vol. 24
Availability: No items available.
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