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

Parkinson's disease with camptocormia

伴有躯干前屈的帕金森病

Bloch, F; Houeto, J L; Tezenas du Montcel, S; Bonneville, F; Etchepare, F; Welter, M L; Rivaud-Pechoux, S; Hahn-Barma, V; Maisonobe, T; Behar, C; Lazennec, J Y; Kurys, E; Arnulf, I; Bonnet, A M; Agid, Y

Familial inflammatory inclusion body myositis

家族性炎症性包涵体肌炎

Ranque-Francois, B; Maisonobe, T; Dion, E; Piette, J-C; Chauveheid, M-P; Amoura, Z; Papo, T

Increased soluble p55 and p75 tumour necrosis factor-alpha receptors in patients with hepatitis C-associated mixed cryoglobulinaemia.

丙型肝炎相关混合型冷球蛋白血症患者体内可溶性 p55 和 p75 肿瘤坏死因子-α 受体增加

Kaplanski G, Marin V, Maisonobe T, Sbai A, Farnarier C, Ghillani P, Thirion X, Durand J M, Harlé J R, Bongrand P, Piette J C, Cacoub P

Hepatitis C virus infection with peripheral neuropathy is not always associated with cryoglobulinaemia

丙型肝炎病毒感染伴周围神经病变并不总是伴有冷球蛋白血症。

Lidove, O; Cacoub, P; Maisonobe, T; Servan, J; Thibault, V; Piette, J C; Léger, J M

Familial macrophagic myofasciitis

家族性巨噬细胞肌筋膜炎

Amoura, Z; Costedoat, N; Maisonobe, T; Godeau, P; Piette, J C

Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate gene

在一个黎巴嫩近亲结婚的大家族中,将常染色体隐性遗传性脱髓鞘性夏科-马里-图斯病的新基因位点定位到19q13.1-13.3:排除MAG作为候选基因

Delague, V; Bareil, C; Tuffery, S; Bouvagnet, P; Chouery, E; Koussa, S; Maisonobe, T; Loiselet, J; Mégarbané, A; Claustres, M