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

An unusual presentation of strongyloidiasis in a patient on chronic dialysis causing clinical deterioration

慢性透析患者出现罕见的粪类圆线虫病表现,导致临床病情恶化

Fofana, Aboubacar Sidiki; Samaké, Magara; Sy, Seydou; Maiga, Hamma; Sadessi, Modibo; Diallo, Adama; Djiguiba, Youssouf Singadou Ousmane; Yalcouyé, Abdoulaye; Kamian, Youssouf; Yattara, Hamadoun; Fongoro, Saharé

Functional Characterization of Splice Variants in the Diagnosis of Albinism

白化病诊断中剪接变异体的功能表征

Modibo Diallo,Cécile Courdier,Elina Mercier,Angèle Sequeira,Alicia Defay-Stinat,Claudio Plaisant,Shahram Mesdaghi,Daniel Rigden,Sophie Javerzat,Eulalie Lasseaux,Laetitia Bourgeade,Séverine Audebert-Bellanger,Hélène Dollfus,Smail Hadj-Rabia,Fanny Morice-Picard,Manon Philibert,Mohamed Kole Sidibé,Vasily Smirnov,Ousmane Sylla,Vincent Michaud,Benoit Arveiler

First Malian series of surgery for rheumatic valve disease: opening of the centre, clinical features and peri-operative realities

马里首例风湿性瓣膜病手术:中心成立、临床特点及围手术期实际情况

Coulibaly, Mahamadoun; Koita, Siriman A; Doumbia, Modibo; Diallo, Binta; Traore, Salia I; Diarra, Baba I; Coulibaly, Brehima; Daffe, Sanoussy; Maiga, Asmaou; Toure, Mamadou; Zongo, Rakiswendé A; Fofana, Gaoussou; Beye, Seydina A; Diallo, Boubacar; Diarra, Mamadou B; Diango, Djibo M; Coulibaly, Youssouf

BLOC1S5 pathogenic variants cause a new type of Hermansky-Pudlak syndrome

BLOC1S5 致病变异导致一种新型 Hermansky-Pudlak 综合征

Perrine Pennamen, Linh Le, Angèle Tingaud-Sequeira, Mathieu Fiore, Anne Bauters, Nguyen Van Duong Béatrice, Valentine Coste, Jean-Claude Bordet, Claudio Plaisant, Modibo Diallo, Vincent Michaud, Aurélien Trimouille, Didier Lacombe, Eulalie Lasseaux, Cédric Delevoye, Fanny Morice Picard, Bruno Delobe

Diabetic polyneuropathy with/out neuropathic pain in Mali: A cross-sectional study in two reference diabetes treatment centers in Bamako (Mali), Western Africa

马里糖尿病性多发性神经病伴/不伴神经性疼痛:一项在西非马里巴马科两家糖尿病治疗中心开展的横断面研究

Maiga, Youssoufa; Diallo, Salimata; Konipo, Fatoumata Dite Nènè; Sangho, Oumar; Sangaré, Modibo; Diallo, Seybou H; Mahamadou, Saliou; Péréon, Yann; Giumelli, Bernard; Coulibaly, Awa; Daou, Mariam; Traoré, Zoumana; Sow Sylla, Djeneba; Albakaye, Mohamed; Guinto, Cheick Oumar; Ouologem, Madani; Sissoko, Adama S; Traoré, Hamar A; Coulibaly, Souleymane Papa; Damier, Philippe; Attal, Nadine; Nizard, Julien

Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12

遗传性痉挛性截瘫43型(SPG43)是由C19orf12基因突变引起的。

Landouré, Guida; Zhu, Peng-Peng; Lourenço, Charles M; Johnson, Janel O; Toro, Camilo; Bricceno, Katherine V; Rinaldi, Carlo; Meilleur, Katherine G; Sangaré, Modibo; Diallo, Oumarou; Pierson, Tyler M; Ishiura, Hiroyuki; Tsuji, Shoji; Hein, Nichole; Fink, John K; Stoll, Marion; Nicholson, Garth; Gonzalez, Michael A; Speziani, Fiorella; Dürr, Alexandra; Stevanin, Giovanni; Biesecker, Leslie G; Accardi, John; Landis, Dennis M D; Gahl, William A; Traynor, Bryan J; Marques, Wilson Jr; Züchner, Stephan; Blackstone, Craig; Fischbeck, Kenneth H; Burnett, Barrington G