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Nima Parvaneh

tehran university of medical sciences

43H指数
231论文数
6.0K被引数
收录论文 68
发表时间
Exploring the Landscape of Food Allergies in Pediatric Atopic Dermatitis: A Cross-Sectional Study in Iran探索伊朗儿科特应性皮炎中的食物过敏状况:一项横断面研究
err2026-01-01
err0
PREAI
errMahdavi, Mohadese; Gharagozlou, Saber; Movahedi, Masoud; Parvaneh, Nima; Kalantari, Arash; Khorshidi, Mohadese Sadat Mousavi; Shokri, Mehdi; Alizadeh, Fatemeh; Movahedi, Mahshid; Gharagozlou, Mohammad
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The neurologic face of X-linked lymphoproliferative syndrome type 1: a systematic reviewX连锁淋巴增殖综合征1型的神经学表现:一项系统综述
err2025-10-23
err0
errOAAI
errErta Rajabi; Saber Gharagozlou; Kousha Farhadi; Moeinadin Safavi; Fatemeh Zamani; Abdolreza Javadi; Zahra Rahemi; Parastoo Rostami; Nima Parvaneh
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Thrombocytopenia in patients with inborn errors of immunity免疫性先天性错误患者的血小板减少症
err2025-10-03
err0
errOAAI
errSaba Fekrvand; Maryam Mohtashami; Negin Sanadgol; Helia Salehi; Najmeh Nameh Goshay Fard; Ehsan Khoshnezhad Afkham; Zahra Chavoshzadeh; Nima Parvaneh; Seyed Alireza Mahdaviani; Samin Sharafian; Sahar Barzamini; Hamid Ahanchian; Arash Kalantari; Alireza Shafiei; Marzieh Tavakol; Farhad Abolnezhadian; Mina Kianmanesh Rad; Gholamreza Hassanpour; Taher Cheraghi; Amir Salehi Farid; Samaneh Delavari; Hassan Abolhassani; Nima Rezaei; Reza Yazdani
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Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants新生儿糖尿病是因隐性NARS2变异引起的COXPD-24的一个显著特征。
err2025-08-31
err0
errOAAI
errRussell Donis; Matthew N. Wakeling; Nicola Jeffery; Molly Govier; Matthew B. Johnson; Samar Sabir Hassan; Mohammed Ahmed Abdullah; Khadiga Yehia Elsayed Eltonbary; Nima Parvaneh; Mahsa M. Amoli; Farzaneh Abbasi; Selin Elmaoğulları; Semra Çetinkaya; Kubra Gunes; Meltem Tayfun; Hanieh Yaghootkar; Andrew T. Hattersley; Sarah E. Flanagan; Elisa De Franco
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Hematopoietic Stem Cell Transplantation for C1q Deficiency: A Study on Behalf of the EBMT Inborn Errors Working Party
err2024-10-29
err0
errOAAI
errBuso, Helena; Adam, Etai; Arkwright, Peter D.; Bhattad, Sagar; Hamidieh, Amir Ali; Behfar, Maryam; Belot, Alexandre; Benezech, Sarah; Chan, Alice Y.; Crow, Yanick J.; Dvorak, Christopher C.; Flinn, Aisling M.; Kapoor, Urvi; Lankester, Arjan; Kobayashi, Masao; Matsumura, Risa; Mottaghipisheh, Hadi; Okada, Satoshi; Ouachee, Marie; Parvaneh, Nima; Ramprakash, Stalin; Satwani, Prakash; Sharafian, Samin; Triaille, Clement; Wynn, Robert F.; Movahedi, Nasim; Ziaee, Vahid; Williams, Eleri; Slatter, Mary; Gennery, Andrew R.
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A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease
err2024-09-13
err0
errOAAI
errMolitor, Anne; Lederle, Alexandre; Radosavljevic, Mirjana; Sapuru, Vinay; Zavorka Thomas, Megan E.; Yang, Jianying; Shirin, Mahsa; Collin-Bund, Virginie; Jerabkova-Roda, Katerina; Miao, Zhichao; Bernard, Alice; Rolli, Veronique; Grenot, Pierre; Castro, Carla Noemi; Rosenzwajg, Michelle; Lewis, Elyssa G.; Person, Richard; Esperon-Moldes, Uxia-Saraiva; Kaare, Milja; Nokelainen, Pekka T.; Batzir, Nurit Assia; Hoffer, Gal Zaks; Paul, Nicodeme; Stemmelen, Tristan; Naegely, Lydie; Hanauer, Antoine; Bibi-Triki, Sabrina; Gruen, Sarah; Jung, Sophie; Busnelli, Ignacio; Tripolszki, Kornelia; Al-Ali, Ruslan; Ordonez, Natalia; Bauer, Peter; Song, Eunkyung; Zajo, Kristin; Partida-Sanchez, Santiago; Robledo-Avila, Frank; Kumanovics, Attila; Louzoun, Yoram; Hirschler, Aurelie; Pichot, Angelique; Toker, Ori; Mejia, Cesar Andres Munoz; Parvaneh, Nima; Knapp, Esther; Hersh, Joseph H.; Kenney, Heather; Delmonte, Ottavia M.; Notarangelo, Luigi D.; Goetz, Jacky G.; Kahwash, Samir B.; Carapito, Christine; Bajwa, Rajinder P. S.; Thomas, Caroline; Ehl, Stephan; Isidor, Bertrand; Carapito, Raphael; Abraham, Roshini S.; Hite, Richard K.; Marcus, Nufar; Bertoli-Avella, Aida; Bahram, Seiamak
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Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect (vol 221, e20221122, 2024)
err2024-05-21
err0
errOAAI
errKoegl, Tamara; Chang, Hsin-Fang; Staniek, Julian; Chiang, Samuel C. C.; Thoulass, Gudrun; Lao, Jessica; Weissert, Kristoffer; Dettmer-Monaco, Viviane; Geiger, Kerstin; Manna, Paul T.; Beziat, Vivien; Momenilandi, Mana; Tu, Szu-Min; Keppler, Selina J.; Pattu, Varsha; Wolf, Philipp; Kupferschmid, Laurence; Tholen, Stefan; Covill, Laura E.; Ebert, Karolina; Straub, Tobias; Gross, Miriam; Gather, Ruth; Engel, Helena; Salzer, Ulrich; Schell, Christoph; Maier, Sarah; Lehmberg, Kai; Cornu, Tatjana I.; Pircher, Hanspeter; Shahrooei, Mohammad; Parvaneh, Nima; Elling, Roland; Rizzi, Marta; Bryceson, Yenan T.; Ehl, Stephan; Aichele, Peter; Ammann, Sandra
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Patients and mice with deficiency in the SNARE protein SYNTAXIN-11 have a secondary B cell defect
err2024-05-09
err1
errOAAI
errKoegl, Tamara; Chang, Hsin-Fang; Staniek, Julian; Chiang, Samuel C. C.; Thoulass, Gudrun; Lao, Jessica; Weissert, Kristoffer; Dettmer-Monaco, Viviane; Geiger, Kerstin; Manna, Paul T.; Beziat, Vivien; Momenilandi, Mana; Tu, Szu-Min; Keppler, Selina J.; Pattu, Varsha; Wolf, Philipp; Kupferschmid, Laurence; Tholen, Stefan; Covill, Laura E.; Ebert, Karolina; Straub, Tobias; Gross, Miriam; Gather, Ruth; Engel, Helena; Salzer, Ulrich; Schell, Christoph; Maier, Sarah; Lehmberg, Kai; Cornu, Tatjana I.; Pircher, Hanspeter; Shahrooei, Mohammad; Parvaneh, Nima; Elling, Roland; Rizzi, Marta; Bryceson, Yenan T.; Ehl, Stephan; Aichele, Peter; Ammann, Sandra
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Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiency双等位基因人SHARPIN功能丧失诱导自身炎症和免疫缺陷
err2024-04-12
err3
PREAI
errOda, Hirotsugu; Manthiram, Kalpana; Chavan, Pallavi Pimpale; Rieser, Eva; Veli, Oenay; Kaya, Oeykue; Rauch, Charles; Nakabo, Shuichiro; Kuehn, Hye Sun; Swart, Mariel; Wang, Yanli; Celik, Nisa Ilgim; Molitor, Anne; Ziaee, Vahid; Movahedi, Nasim; Shahrooei, Mohammad; Parvaneh, Nima; Alipour-Olyei, Nasrin; Carapito, Raphael; Xu, Qin; Preite, Silvia; Beck, David B.; Chae, Jae Jin; Nehrebecky, Michele; Ombrello, Amanda K.; Hoffmann, Patrycja; Romeo, Tina; Deuitch, Natalie T.; Matthiasardottir, Brynja; Mullikin, James; Komarow, Hirsh; Stoddard, Jennifer; Niemela, Julie; Dobbs, Kerry; Sweeney, Colin L.; Anderton, Holly; Lawlor, Kate E.; Yoshitomi, Hiroyuki; Yang, Dan; Boehm, Manfred; Davis, Jeremy; Mudd, Pamela; Randazzo, Davide; Tsai, Wanxia Li; Gadina, Massimo; Kaplan, Mariana J.; Toguchida, Junya; Mayer, Christian T.; Rosenzweig, Sergio D.; Notarangelo, Luigi D.; Iwai, Kazuhiro; Silke, John; Schwartzberg, Pamela L.; Boisson, Bertrand; Casanova, Jean-Laurent; Bahram, Seiamak; Rao, Anand Prahalad; Peltzer, Nieves; Walczak, Henning; Lalaoui, Najoua; Aksentijevich, Ivona; Kastner, Daniel L.
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Analysis of Lymphocyte and Clinical Profile in Nonmonogenic Common Variable Immunodeficiency Patients With and Without Class Switch Recombination Defect
err2023-12-13
err0
errOAAI
errZavareh, F. Tofighi; Mirshafiey, A.; Yazdani, R.; Keshtkar, A. A.; Abolhassani, H.; Kiaee, F.; Parvaneh, N.; Shariat, M.; Rezaei, N.; Aghamohammadi, A.
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Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population
err2023-08-16
err4
errOAAI
errKhorshidi, Mohadese Sadat Mousavi; Seeleuthner, Yoann; Chavoshzadeh, Zahra; Behfar, Maryam; Hamidieh, Amir Ali; Alimadadi, Hosein; Sherkat, Roya; Momen, Tooba; Behniafard, Nasrin; Eskandarzadeh, Shabnam; Mansouri, Mahboubeh; Behnam, Mahdiyeh; Mahdavi, Mohadese; Zadeh, Maryam Heydarazad; Shokri, Mehdi; Alizadeh, Fatemeh; Movahedi, Mahshid; Momenilandi, Mana; Keramatipour, Mohammad; Casanova, Jean-Laurent; Cobat, Aurelie; Abel, Laurent; Shahrooei, Mohammad; Parvaneh, Nima
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Clinical and immunological characteristics of 69 leukocyte adhesion deficiency-I patients
err2023-07-14
err1
PREAI
errFazlollahi, Mohammad Reza; Hamidieh, Amir Ali; Moradi, Leila; Shoormati, Raheleh Shokouhi; Sabetkish, Nastaran; Esmaeili, Behnaz; Badalzadeh, Mohsen; Alizadeh, Zahra; Shamlou, Somayeh; Movahedi, Masoud; Mahloujirad, Maryam; Razaghian, Anahita; Arshi, Saba; Gharagozlou, Mohammad; Kalantari, Arash; Bemanian, Mohammad Hassan; Safari, Mojgan; Arani, Marzieh Heidarzadeh; Nabavi, Mohammad; Parvaneh, Nima; Sadeghi-Shabestari, Mahnaz; Behfar, Maryam; Behniafard, Nasrin; Sherkat, Roya; Ahmadian Heris, Javad; Shariat, Mansoureh; Radmehr, Roshanak; Houshmand, Massoud; Kazemnejad, Anoshirvan; Molitor, Anne; Carapito, Raphael; Bahram, Seiamak; Pourpak, Zahra; Moin, Mostafa
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Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling遗传性ARPC5突变导致放线菌病损害细胞运动并破坏细胞因子信号传导
err2023-06-22
err7
errOAAI
errNunes-Santos, Cristiane J.; Kuehn, HyeSun; Boast, Brigette; Hwang, SuJin; Kuhns, Douglas B.; Stoddard, Jennifer; Niemela, Julie E.; Fink, Danielle L.; Pittaluga, Stefania; Abu-Asab, Mones; Davies, John S.; Barr, Valarie A.; Kawai, Tomoki; Delmonte, Ottavia M.; Bosticardo, Marita; Garofalo, Mary; Carneiro-Sampaio, Magda; Somech, Raz; Gharagozlou, Mohammad; Parvaneh, Nima; Samelson, Lawrence E.; Fleisher, Thomas A.; Puel, Anne; Notarangelo, Luigi D.; Boisson, Bertrand; Casanova, Jean-Laurent; Derfalvi, Beata; Rosenzweig, Sergio D.
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Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A)
err2023-06-14
err6
errOAAI
errBrauer, Nina; Maruta, Yuto; Lisci, Miriam; Strege, Katharina; Oschlies, Ilske; Nakamura, Hikari; Boehm, Svea; Lehmberg, Kai; Brandhoff, Leon; Ehl, Stephan; Parvaneh, Nima; Klapper, Wolfram; Fukuda, Mitsunori; Griffiths, Gillian M.; Hennies, Hans Christian; Niehues, Tim; Ammann, Sandra
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Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease人类生殖系杂合功能增益STAT6变体导致严重的过敏性疾病
err2023-03-08
err41
errOAAI
errSharma, Mehul; Leung, Daniel; Momenilandi, Mana; Jones, Lauren C. W.; Pacillo, Lucia; James, Alyssa E.; Murrell, Jill R.; Delafontaine, Selket; Maimaris, Jesmeen; Vaseghi-Shanjani, Maryam; Del Bel, Kate L.; Lu, Henry Y.; Chua, Gilbert T.; Di Cesare, Silvia; Fornes, Oriol; Liu, Zhongyi; Di Matteo, Gigliola; Fu, Maggie P.; Amodio, Donato; Tam, Issan Yee San; Chan, Gavin Shueng Wai; Sharma, Ashish A.; Dalmann, Joshua; van der Lee, Robin; Blanchard-Rohner, Geraldine; Lin, Susan; Philippot, Quentin; Richmond, Phillip A.; Lee, Jessica J.; Matthews, Allison; Seear, Michael; Turvey, Alexandra K.; Philips, Rachael L.; Brown-Whitehorn, Terri F.; Gray, Christopher J.; Izumi, Kosuke; Treat, James R.; Wood, Kathleen H.; Lack, Justin; Khleborodova, Asya; Niemela, Julie E.; Yang, Xingtian; Liang, Rui; Kui, Lin; Wong, Christina Sze Man; Poon, Grace Wing Kit; Hoischen, Alexander; van der Made, Caspar I.; Yang, Jing; Chan, Koon Wing; Rosa Duque, Jaime Sou Da; Lee, Pamela Pui Wah; Ho, Marco Hok Kung; Chung, Brian Hon Yin; Le, Huong Thi Minh; Yang, Wanling; Rohani, Pejman; Fouladvand, Ali; Rokni-Zadeh, Hassan; Changi-Ashtiani, Majid; Miryounesi, Mohammad; Puel, Anne; Shahrooei, Mohammad; Finocchi, Andrea; Rossi, Paolo; Rivalta, Beatrice; Cifaldi, Cristina; Novelli, Antonio; Passarelli, Chiara; Arasi, Stefania; Bullens, Dominique; Sauer, Kate; Claeys, Tania; Biggs, Catherine M.; Morris, Emma C.; Rosenzweig, Sergio D.; O'Shea, John J.; Wasserman, Wyeth W.; Bedford, H. Melanie; van Karnebeek, Clara D. M.; Palma, Paolo; Burns, Siobhan O.; Meyts, Isabelle; Casanova, Jean-Laurent; Lyons, Jonathan J.; Parvaneh, Nima; Nguyen, Anh Thi Van; Cancrini, Caterina; Heimall, Jennifer; Ahmed, Hanan; McKinnon, Margaret L.; Lau, Yu Lung; Beziat, Vivien; Turvey, Stuart E.
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Human IL-23 is essential for IFN-y-dependent immunity to mycobacteria
err2023-02-03
err35
errOAAI
errPhilippot, Quentin; Ogishi, Masato; Bohlen, Jonathan; Puchan, Julia; Arias, Andres Augusto; Nguyen, Tina; Martin-Fernandez, Marta; Conil, Clement; Rinchai, Darawan; Momenilandi, Mana; Mandaviani, Seyed Alireza; Keramatipour, Mohammad; Rosain, Jeremie; Yang, Rui; Khan, Taushif; Neehus, Anna-Lena; Materna, Marie; Han, Ji Eun; Peel, Jessica; Mele, Federico; Weisshaar, Marc; Jovic, Sandra; Bastard, Paul; Levy, Romain; Le Voyer, Tom; Zhang, Peng; Renkilaraj, Majistor Raj Luxman Maglorius; Arango-Franco, Carlos A.; Pelham, Simon; Seeleuthner, Yoann; Pochon, Mathieu; Ata, Manar Mahmoud Ahmad; Al Ali, Fatima; Migaud, Melanie; Soudee, Camille; Kochetkov, Tatiana; Molitor, Anne; Carapito, Raphael; Bahram, Seiamak; Boisson, Bertrand; Fieschi, Claire; Mansouri, Davood; Marr, Nico; Okada, Satoshi; Shahrooei, Mohammad; Parvaneh, Nima; Chavoshzadeh, Zahra; Cobat, Aurelie; Bogunovic, Dusan; Abel, Laurent; Tangye, Stuart G.; Ma, Cindy S.; Beziat, Vivien; Sallusto, Federica; Boisson-Dupuis, Stephanie; Bustamante, Jacinta; Casanova, Jean-Laurent; Puel, Anne
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Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis
err2022-11-03
err11
errOAAI
errOgishi, Masato; Yang, Rui; Rodriguez, Remy; Golec, Dominic P.; Martin, Emmanuel; Philippot, Quentin; Bohlen, Jonathan; Pelham, Simon J.; Arias, Andres Augusto; Khan, Taushif; Ata, Manar; Al Ali, Fatima; Rozenberg, Flore; Kong, Xiao-Fei; Chrabieh, Maya; Laine, Candice; Lei, Wei-Te; Han, Ji Eun; Seeleuthner, Yoann; Kaul, Zenia; Jouanguy, Emmanuelle; Beziat, Vivien; Youssefian, Leila; Vahidnezhad, Hassan; Rao, V. Koneti; Neven, Benedicte; Fieschi, Claire; Mansouri, Davood; Shahrooei, Mohammad; Pekcan, Sevgi; Alkan, Gulsum; Emiroglu, Melike; Tokgoez, Hueseyin; Uitto, Jouni; Hauck, Fabian; Bustamante, Jacinta; Abel, Laurent; Keles, Sevgi; Parvaneh, Nima; Marr, Nico; Schwartzberg, Pamela L.; Latour, Sylvain; Casanova, Jean-Laurent; Boisson-Dupuis, Stephanie
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Adenosine Deaminase (ADA) Deficiency: Report of Six New Cases and Reappraisal of Cutaneous Hypermelanosis as an Early Feature
err2022-07-29
err1
PREAI
errSharafian, Samin; Jacomelli, Gabriella; Tamizifar, Banafshe; Shahrooei, Mohammad; Parvaneh, Nima
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Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variants
err2022-01-06
err4
errOAAI
errSetoodeh, Aria; Panjeh-Shahi, Samareh; Bahmani, Fariba; Vand-Rajabpour, Fatemeh; Jalilian, Nazanin; Sayarifard, Fatemeh; Abbasi, Farzaneh; Sayarifard, Azadeh; Rostami, Parastoo; Parvaneh, Nima; Akhavan-Niaki, Haleh; Ahmadifard, Mohamadreza; Tabrizi, Mina
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