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

The expanding clinical and genetic spectrum of DYNC1H1-related disorders

DYNC1H1相关疾病的临床和遗传谱不断扩大

Möller, Birk; Becker, Lena-Luise; Saffari, Afshin; Afenjar, Alexandra; Coci, Emanuele G; Williamson, Rachel; Ward-Melver, Catherine; Gibaud, Marc; Sedláčková, Lucie; Laššuthová, Petra; Libá, Zuzana; Vlčková, Markéta; William, Nancy; Klee, Eric W; Gavrilova, Ralitza H; Lévy, Jonathan; Capri, Yline; Scavina, Mena; Körner, Robert Walter; Valivullah, Zaheer; Weiß, Claudia; Möller, Greta Marit; Frazier, Zoë; Roberts, Amy; Gener, Blanca; Scala, Marcello; Striano, Pasquale; Zara, Federico; Thiel, Moritz; Sinnema, Margje; Kamsteeg, Erik-Jan; Donkervoort, Sandra; Duboc, Veronique; Zaafrane-Khachnaoui, Khaoula; Elkhateeb, Nour; Selim, Laila; Margot, Henri; Marin, Victor; Beneteau, Claire; Isidor, Bertrand; Cogne, Benjamin; Keren, Boris; Küsters, Benno; Beggs, Alan H; Sveden, Abigail; Chopra, Maya; Genetti, Casie A; Nicolai, Joost; Dötsch, Jörg; Koy, Anne; Bönnemann, Carsten G; von der Hagen, Maja; von Kleist-Retzow, Jürgen-Christoph; Voermans, Nicol C; Jungbluth, Heinz; Dafsari, Hormos Salimi

Psychological and behavioral characterization of suicide ideators and suicide attempters in adolescence

青少年自杀意念者和自杀未遂者的心理和行为特征

Coci, Chiara; Invernizzi, Roberta; Capone, Luca; Casini, Erica; Orlandi, Marika; Galli, Paola; Rossi, Ilaria; Martinelli, Ottaviano; Borgatti, Renato; Mensi, Martina Maria

Family Dysfunctional Interactive Patterns and Alexithymia in Adolescent Patients with Restrictive Eating Disorders

家庭功能失调的互动模式与青少年限制性饮食障碍患者的述情障碍

Coci, Chiara; Provenzi, Livio; De Giorgis, Valentina; Borgatti, Renato; Chiappedi, Matteo; Mensi, Martina Maria; On Behalf Of The Mondino Foundation Eating Disorders Clinical And Research Group

Expanding the phenotype of TAB2 variants and literature review

扩展TAB2变异体的表型及文献综述

Woods, Emily; Marson, Imogen; Coci, Emanuele; Spiller, Michael; Kumar, Ajith; Brady, Angela; Homfray, Tessa; Fisher, Richard; Turnpenny, Peter; Rankin, Julia; Kanani, Farah; Platzer, Konrad; Ververi, Athina; Emmanouilidou, Eleftheria; Bourboun, Nourxan; Giannakoulas, George; Balasubramanian, Meena

(PO-172) COVID-19 Catatonia: A Review and Update After One Year

(PO-172)新冠肺炎紧张症:一年后的回顾与更新

Son, Jung-Woo; Rogantini, C; Orlandi, M; Provenzi, L; Chiappedi, M; Coci, C; Criscuolo, M; Castiglioni, M; Zanna, V; Borgatti, R; Mensi, M; Watanabe, K; Moriguchi, Y; Ren, H; Mendez, MA; San Jose Caceres, A; Oakley, B; Murphy, D; Arango, C; Parellada, M; Canitano, R; Quoidbach, V; Maia, A; De Souza Queiroz, J; Barahona-Correa, B; Oliveira, J; Oliveira-Maia, AJ; Urbina Trevino, L; Von Mücke-Heim, I-A; Deussing, J; Orlandi, M; Iorio, M; Rogantini, C; Vecchio, A; Coci, C; Casini, E; Borgatti, R; Mensi, M; Baglioni, V; Cesario, S; Gigliotti, F; Galosi, S; Maggio, C Di; Ferrara, M; Leuzzi, V; Santo, F Di; Zinchuk, M; Beghi, M; Beghi, E; Kustov, G; Pashnin, E; Voinova, N; Avedisova, A; Guekht, A; Geffen, T; Smallwood, J; Finke, C; Sjoerds, Z; Schlagenhauf, F; Blum, Austin W; Leo, Hannah; Ihle, Eva C; Cooper, Joseph; Datta, Vivek

Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes

更正:CANPMR综合征和1p32-p31染色体缺失综合征同时存在于两名受CAMTA1和NFIA基因单倍体不足影响的亲缘个体中。

Coci, Emanuele G; Koehler, Udo; Liehr, Thomas; Stelzner, Armin; Fink, Christian; Langen, Hendrik; Riedel, Joachim

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

双等位基因 MADD 变异可导致一系列表型,从发育迟缓到多系统疾病

Pauline E Schneeberger, Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy, Daniela Buhas, Stephanie Fox, Jane Juusola, Majid Alfadhel, Bryn D Webb, Emanuele G Coci, Rami Abou Jamra, Manuela Siekmeyer, Saskia Biskup, Corina Heller, Esther M Maier, Poupak Javaher-Haghighi,

The diagnostic ability of core needle biopsy in nodular thyroid disease

空芯针穿刺活检在结节性甲状腺疾病诊断中的能力

Aysan, E; Kiran, T; Idiz, U O; Guler, B; Akbulut, H; Kunduz, E; Arici, S; Kadakal, G; Ozgor, M; Coci, K

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes

CANPMR 综合征和 1p32-p31 染色体缺失综合征同时存在于两个相关个体中,且这两个个体同时受到 CAMTA1 和 NIFA 基因单倍体不足的影响

Emanuele G Coci, Udo Koehler, Thomas Liehr, Armin Stelzner, Christian Fink, Hendrik Langen, Joachim Riedel

Ecology and Distribution of Thaumarchaea in the Deep Hypolimnion of Lake Maggiore

马焦雷湖深水层中奇古菌的生态与分布

Coci, Manuela; Odermatt, Nina; Salcher, Michaela M; Pernthaler, Jakob; Corno, Gianluca