日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Diagnostic challenge in a series of eleven patients with hyper IgE syndromes

11 例高 IgE 综合征患者的诊断挑战

Roukaya Yaakoubi, Najla Mekki, Imen Ben-Mustapha, Leila Ben-Khemis, Asma Bouaziz, Ilhem Ben Fraj, Jamel Ammar, Agnès Hamzaoui, Hamida Turki, Lobna Boussofara, Mohamed Denguezli, Samir Haddad, Monia Ouederni, Mohamed Bejaoui, Koon Wing Chan, Yu Lung Lau, Fethi Mellouli, Mohamed-Ridha Barbouche, Merie

Vaccine-induced dermatomyositis following COVID-19 vaccination

新冠疫苗接种后引起的疫苗诱发性皮肌炎

Chaima, Kouki; Mariem, Amouri; Sana, Bouzid; Khadija, Sellami; Mariem, Rekik; Massara, Baklouti; Emna, Bahloul; Sonia, Boudaya; Abderrahman, Masmoudi; Hamida, Turki

Lichen planus pigmentosus post COVID-19-vaccination: A case report with literature review

新冠疫苗接种后出现色素性扁平苔藓:病例报告及文献综述

Chaima, Kouki; Fatma, Hammami; Nadine, Kammoun; Chahir, Kammoun; Emna, Bahloul; Khadija, Sellami; Mariem, Amouri; Sonia, Boudaya; Abderrahman, Masmoudi; Tahya, Boudawara; Hamida, Turki

Kaposiform hemangioendothelioma with fatal income: Kasabach-Merritt phenomenon and hypercalcemia

伴有致命性收入的卡波西样血管内皮瘤:卡萨巴赫-梅里特现象和高钙血症

Massara, Baklouti; Mariem, Rekik; Emna, Bahloul; Meriam, Triki; Faiza, Safi; Sonia, Boudaya; Meriem, Amouri; Lamia, Gargouri; Tahia, Sellami; Hamida, Turki

Multiple asymptomatic papules following breast cancer treatment

乳腺癌治疗后出现多发性无症状丘疹

Chaima, Kouki; Khadija, Sellami; Emna, Bahloul; Emna, Mnif; Soumaya, Graja; Nadine, Kammoun; Naourez, Gouiaa; Tahya, Boudawara; Hamida, Turki

Fat necrosis: A neglected side effect of intramuscular injections

脂肪坏死:肌肉注射常被忽视的副作用

Chaima, Kouki; Mariem, Amouri; Emna, Bahloul; Slim, Charfi; Fatma, Hammemi; Tahya, Boudawara; Hamida, Turki

S4.5d Comparing the diagnostic performance of the commonly used eumycetoma diagnostic tests using sequencing of the internally transcribed spacer region as the gold standard

S4.5d 以内部转录间隔区测序为金标准,比较常用真菌瘤诊断试验的诊断性能

Chaima, Kouki; Mariem, Amouri; Khadija, Sellami; Rim, Kallel; Emna, Bahloul; Tahya, Boudawa; Hamida, Turki; Siddig, Emmanuel; Nyuykonge, Bertrand; Mhmoud, Najwa; Abdallah, Omnia; Bahar, Mustafa; Ahmed, Eiman; Nyaoke, Borna; Zijlstra, Ed; Verbon, Annelies; Bakhiet, Sahar; Fahal, Ahmed; van de Sande, Wendy

A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation

PLCD1 中的单等位基因双重打击机制解释了遗传性毛囊囊肿形成的遗传发病机制

Steffen Hörer, Slaheddine Marrakchi, Franz P W Radner, Gerd Zolles, Lisa Heinz, Thomas O Eichmann, Cristina Has, Pavel Salavei, Nadia Mahfoudh, Hamida Turki, Andreas D Zimmer, Judith Fischer

Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans

SULT2B1 基因突变导致人类常染色体隐性先天性鱼鳞病

Lisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, Julie Christiansen, Hamida Turki, Marc-Alexander Rauschendorf, Mark Lathrop, Ingrid Hausser, Andreas D Zimmer, Judith Fischer

Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans

CERS3 基因突变导致人类常染色体隐性先天性鱼鳞病

Franz P W Radner, Slaheddine Marrakchi, Peter Kirchmeier, Gwang-Jin Kim, Florence Ribierre, Bourane Kamoun, Leila Abid, Michael Leipoldt, Hamida Turki, Werner Schempp, Roland Heilig, Mark Lathrop, Judith Fischer