Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Rim Chaabouni"'
Publikováno v:
Clinical Case Reports, Vol 11, Iss 4, Pp n/a-n/a (2023)
Abstract Considering the rarity and underdiagnoses of this disorder, a pigmented and hyperkeratotic skin lesion located on the trunk, resembling to acanthosis nigricans should always be investigated for terra firma‐forme dermatosis (TFFD) and thus
Externí odkaz:
https://doaj.org/article/4b6300dd1bfe4a0cbf8a873df5b1fc39
Autor:
Mariem Ennouri, Andreas D. Zimmer, Emna Bahloul, Rim Chaabouni, Slaheddine Marrakchi, Hamida Turki, Faiza Fakhfakh, Noura Bougacha-Elleuch, Judith Fischer
Publikováno v:
BMC Medical Genomics, Vol 15, Iss 1, Pp 1-10 (2022)
Abstract Background Ichthyosis is a heterogeneous group of Mendelian cornification disorders that includes syndromic and non-syndromic forms. Autosomal Recessive Congenital Ichthyosis (ARCI) and Ichthyosis Linearis Circumflexa (ILC) belong to non-syn
Externí odkaz:
https://doaj.org/article/c57723e82e6245b4940077ca5311cf91
Autor:
Fatma Hammami, Khadija Sellami, Rim Chaabouni, Sonia Boudaya, Meriem Amouri, Emna Bahloul, Hamida Turki
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract The anal region is an unusual site of Hailey–Hailey disease. It manifests with lichenoid lesions with crusted erosions around the anus. It should be differentiated from condylomata acuminata, extramammary Paget disease, and bowenoid papulo
Externí odkaz:
https://doaj.org/article/55c44860db6e44a8943e1d8eb714f600
Autor:
Fatma Hammami, Makram Koubaa, Mourad Chaari, Rim Chaabouni, Abrakhom Zeyni, Khaoula Rekik, Fatma Smaoui, Mounir Ben Jemaa
Publikováno v:
Asian Pacific Journal of Tropical Medicine, Vol 13, Iss 10, Pp 467-471 (2020)
Rationale: Haemophagocytic lymphohistiocytosis is a rare complication of malaria, which is often misdiagnosed. Patient concerns: A 30-year-old male was admitted to our department for persistent fever, which began after returning from a stay in Guinea
Externí odkaz:
https://doaj.org/article/6e5d915cc2e64d8e84095d8f8c0a1b0a
Autor:
Massara Baklouti, Khadija Sellami, Manel Mellouli, Mariem Rekik, Rim Chaabouni, Abderahmen Masmoudi, Tahya Sellami, Hamida Turki
Publikováno v:
Indian Journal of Dermatology, Vol 68, Iss 1, Pp 122-122 (2023)
Inverted follicular keratosis (IFK) is a rare benign tumour of the follicular infundibulum characterized by exo-endophytic growing. Generally, the diagnosis of IFK is histopathologically made because clinical differentiation from other lesions is dif
Externí odkaz:
https://doaj.org/article/9494257f17944404b3acd16a5b081cdf
Caractérisation du lait de deux races locales de vaches : la Bretonne Pie Noir et la Froment du Léon
Autor:
Catherine HURTAUD, Rim CHAABOUNI, Rémi RESMOND, Guy MIRANDA, Benoît GRAULET, Clémence MORINIÈRE
Publikováno v:
INRAE Productions Animales, Vol 34, Iss 1 (2021)
Malgré un net regain d’intérêt, les références techniques sur les systèmes valorisant les races locales bretonnes sont quasi inexistantes. Les éleveurs comme les restaurateurs s’intéressent à la spécificité des produits issus de ces ra
Externí odkaz:
https://doaj.org/article/dd3cca3ee26e4e5ea37b12edf0ecf775
Autor:
Rim Chaabouni, Chiraz Chaari, Meriem Amouri, Khadija Sellami, Yosra Bouattour, Hamida Turki, Zouheir Bahloul, Tahiya Boudawara
Publikováno v:
Néphrologie & Thérapeutique. 18:136-139
Resume Introduction Les epidermolyses bulleuses dystrophiques recessives representent un groupe de maladies genetiques, caracterisees par une fragilite cutanee et muqueuse, causees par des mutations dans le gene COL7A1. L’amylose AA constitue une c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7738833a95a79065632d7a6e4b4af279
https://doi.org/10.1016/j.nephro.2021.08.005
https://doi.org/10.1016/j.nephro.2021.08.005
Autor:
Rim Chaabouni, Noura Bougacha, Khadija Sellami, Emna Bahloul, Meriem Amouri, Slim Charfi, Slaheddine Marrakchi, Mariam Ennouri, Rim Atheymen, Sonia Boudaya, Hamida Turki
Publikováno v:
International Journal of Dermatology. 60:742-748
Background Hydroxychloroquine (HCQ)-induced acute generalized exanthematous pustulosis (AGEP) is poorly described in the literature. The aim of our study was to characterize the clinical, laboratory, allergological, and genetic features of HCQ-induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::753b89abef950ea1a8516399c818f6ca
https://doi.org/10.1111/ijd.15419
https://doi.org/10.1111/ijd.15419
Publikováno v:
Australasian Journal of Dermatology. 62
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ff6ad009c83bada2355474383cfd5dd
https://doi.org/10.1111/ajd.13569
https://doi.org/10.1111/ajd.13569