Lydie Bürglen - Publications, H-index & Citations

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Lydie Bürglen

no institution name

53H-index

202Paper Count

1.4WCitation Count

Published Papers 93

Publication Date

Highlighting the value of polymyography in childhood onset movement disorders

Frontiers in Neurology

IF2.8

2026-05-28

OAAI

RM Raffaella Moretti †; CR Claudia Ravelli †; YA Yara Ahmar; ND Nathalie Dorison; MD Marie De Salins; DR Diana Rodriguez; KD Kumaran Deiva; AI Anne Isabelle Vermersch; MH Minh Hanh Triboulet; SV Stéphanie Valence; MH Madeleine Harion; LB Lydie Burglen; EA Emmanuelle Apartis ‡; DD Diane Doummar ‡

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Evaluation of the contribution of trio-exome sequencing in selected prenatal indications

Frontiers in Genetics

IF2.8

2026-05-11

OAAI

MC Manon Chretien †; JO Julien Osouf †; CA Carine Abel; AA Alexandra Afenjar; TA Tania Attie-Bitach; EB Elise Brischoux-Boucher; LB Lydie Burglen; NC Nadège Calmels; NC Nicolas Chassaing; TC Thomas Courtin; JD Julian Delanne; MD Martine Doco-Fenzy; CD Christèle Dubourg; BD Benjamin Durand; SE Salima El Chehadeh; LF Laurence Faivre; AG Aurore Garde; EG Emmanuelle Ginglinger; VH Virginie Haushalter; DH Damien Haye; SH Solveig Heide; LH Laurence Heidet; DH Delphine Heron; CJ Clémence Jacquin; LL Laetitia Lambert; JL Jean-Baptiste Lamouche; VL Vincent Laugel; AL Antony Le Bechec; DL Daphné Lehalle; LM Laurence Michel-Calemard; EM Edgar Montoya Ramirez; JM Jean Muller; SO Sylvie Odent; OP Olivier Patat; JP Juliette Piard; CP Céline Poirsier; AP Audrey Putoux; CQ Chloé Quelin; CR Caroline Racine; NS Nicolas Sananes; AS Audrey Schalk; SS Sophie Scheidecker; CT Christel Thauvin-Robinet; SV Stéphanie Valence; AW Anne-Sophie Weingertner; JW Justine Wourms; HD Hélène Dollfus; BG Bénédicte Gerard ‡; CS Caroline Schluth-Bolard ‡; ES Elise Schaefer ‡

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Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders

The Journal of Clinical Endocrinology & Metabolism

IF0

2026-03-11

PREAI

Gwenaëlle Diene; Grégoire Benvegnu; Cathy Brochado; Alice Clerc; Béatrice Jouret; Emilie Montastier; Solange Grunenwald; Christine Poitou; Delphine Heron; Vincent des Portes; David Cohen; Angèle Consoli; Caroline Demily; Lydie Burglen; Alexandra Anfejar; Marion Valette; Maithé Tauber

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Genetic variants in ESRRG are associated with a dominant non-progressive congenital movement disorder with ataxia

The American Journal of Human Genetics

IF0

2025-11-19

PREAI

Brandon Bresack; Laura Renée Kohl; Alexandra Afenjar; Frédérique Audic; Lydie Burglen; Perrine Charles; Nihal Olgac Dundar; Jiddeke van de Kamp; Keren Machol; Pilar Magoulas; Odile Goze-Martineau; Mahdi Motazacker; Heike Philippi; Alejandra Reyes; Omar A.Z. Tutakhel; Aida Bertoli-Avella; Heinrich Sticht; Rami Abou Jamra; Henry Oppermann

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Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function

Nature Genetics

IF29

2025-10-22

OAAI

Reza Asadollahi; Aisha Ahmad; Paranchai Boonsawat; Jasmine Shahanoor Hinzen; Mareike Lohse; Boris Bouazza-Arostegui; Siqi Sun; Tillmann Utesch; Jonas D. Sommer; Dragana Ilic; Murugesh Padmanarayana; Kati Fischermanns; Mrinalini Ranjan; Moritz Boll; Chandran Ka; Amélie Piton; Francesca Mattioli; Bertrand Isidor; Katrin Õunap; Karit Reinson; Monica H. Wojcik; Christian R. Marshall; Saadet Mercimek-Andrews; Naomichi Matsumoto; Noriko Miyake; Bruno de Oliveira Stephan; Rachel Sayuri Honjo; Debora R. Bertola; Chong Ae Kim; Roman Yusupov; Heather C. Mefford; John Christodoulou; Joy Lee; Oliver Heath; Natasha J. Brown; Naomi Baker; Zornitza Stark; Martin Delatycki; Nicole J. Lake; Shimriet Zeidler; Linda Zuurbier; Saskia M. Maas; Chris C. de Kruiff; Farrah Rajabi; Lance H. Rodan; Stephanie A. Coury; Konrad Platzer; Henry Oppermann; Rami Abou Jamra; Skadi Beblo; Caroline Maxton; Robert Śmigiel; Hunter Underhill; Holly Dubbs; Alyssa Rosen; Katherine L. Helbig; Ingo Helbig; Sarah McKeown Ruggiero; Mark P. Fitzgerald; Dennis Kraemer; Carlos E. Prada; Jeffrey Tenney; Parul Jayakar; Sylvia Redon; Jérémie Lefranc; Kevin Uguen; Simone Race; Stephanie Efthymiou; Reza Maroofian; Henry Houlden; Sandra Coppens; Nicolas Deconinck; Balasubramaniem Ashokkumar; Perumal Varalakshmi; Vykunta Raju Gowda K; Fatemeh Eghbal; Ehsan Ghayoor Karimiani; Morteza Heidari; John Neidhardt; Marta Owczarek-Lipska; G. Christoph Korenke; Michael J. Bamshad; Philippe M. Campeau; Anna Lehman; Laura G. Hendon; Ingrid M. Wentzensen; Kristin G. Monaghan; Yanmin Chen; Anna Szuto; Ronald D. Cohn; Ping Yee Billie Au; Christoph Hübner; Felix Boschann; Kandamurugu Manickam; Daniel C. Koboldt; Aboulfazl Rad; Gabriela Oprea; Kristine K. Bachman; Andrea H. Seeley; Emanuele Agolini; Alessandra Terracciano; Piscopo Carmelo; Caleb Bupp; Bethany Grysko; Annick Rein-Rothschild; Bruria Ben Zeev; Amy Margolin; Jennifer Morrison; Aditi Dagli; Elliot Stolerman; Raymond J. Louie; Camerun Washington; Servi J. C. Stevens; Malou Heijligers; Fowzan S. Alkuraya; Jasmin Lisfeld; Axel Neu; Fabíola Paoli Monteiro; André Luiz Santos Pessoa; Antonio Edvan Camelo-Filho; Fernando Kok; Dwight Koeberl; Kacie Riley; Lydie Burglen; Diane Doummar; Bénédicte Héron; Cyril Mignot; Boris Keren; Perrine Charles; Caroline Nava; Felix P. Bernhard; Andrea A. Kühn; Sven Thoms; Ryan D. Morrie; Shila Mekhoubad; Eric M. Green; Sami J. Barmada; Aaron D. Gitler; Olaf Jahn; Jeong Seop Rhee; Christian Rosenmund; Mišo Mitkovski; Heinrich Sticht; Han Sun; Gerald Le Gac; Holger Taschenberger; Nils Brose; Jeremy S. Dittman; Anita Rauch; Noa Lipstein

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CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies

Science Advances

IF12.5

2025-10-17

PREAI

Kamal Khan; Erika Tavares; Katherine Bishara; Aysegul Ozanturk; Leila Qebibo; Stephan Frangakis; Daniel G. Calame; Isabelle Meunier; Béatrice Bocquet; Rafal Ploski; Mohammad Ayman Al Khateeb; Dana Marafi; Luke Mansard; Lena Damaj; Richard A. Lewis; Farid Ullah; Thomas Arbogast; Jackson P. Ogden; Madeleine Harion; Marjolaine Willems; Maha S. Zaki; Tobias Bartolomaeus; Anne-Françoise Roux; James R. Lupski; Malgorzata Rydzanicz; Rami Abou Jamra; Francis Ramond; Elise Heon; Lydie Burglen; Erica E. Davis

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Electrophysiological classification of CACNA1G gene variants associated with neurodevelopmental and neurological disorders

Frontiers in Pharmacology

IF4.8

2025-10-02

OAAI

Amaël Davakan†; Leos Cmarko†; Barbara Ribeiro Oliveira-Mendes; Claire Bernat; Najlae Boulali; Jérôme Montnach; Stephanie E. Vallee; Mary B. Dinulos; Lydie Burglen; Vincent Cantagrel; Norbert Weiss; Sophie Nicole; Arnaud Monteil; Michel De Waard; Philippe Lory

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Attenuated Clinical Forms of Tubulinopathies in Children and Adults: A Series of 24 Individuals

Pediatric Neurology

IF2.1

2025-06-11

OAAI

Meghane Durizot; Lydie Burglen; Catherine Garel; Eléonore Blondiaux; Audrey Riquet; Valentine Floret; Vincent Desportes; Maria Häänpaa; Maria Irene Valenzuela; Anna Maria Pinto; Alessandra Renieri; Michiel Vanneste; Koen Devriendt; Liesbeth de Waele; Lucie Guilbaud; Jean-Marie Jouannic; Madeleine Harion; Thierry Billette de Villemeur; Diana Rodriguez; Emmanuelle Lacaze; Stéphanie Valence

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Atypical ADCY5-related movement disorders: Highlighting adolescent/ adult-onset cervical dystonia

PARKINSONISM & RELATED DISORDERS

IF3.4

2025-03-01

PREAI

Quazza, Floriane; Riant, Florence; Patera, Martina; Suppa, Antonio; Satolli, Sara; Burglen, Lydie; Zech, Michael; Boesch, Sylvia; Indelicato, Elisabetta; Hainque, Elodie; Apartis, Emmanuelle; Rodriguez, Diana; Doummar, Diane; Meneret, Aurelie; Ravelli, Claudia

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The characterization of new de novo CACNA1G variants affecting the intracellular gate of Cav3.1 channel broadens the spectrum of neurodevelopmental phenotypes in SCA42ND

GENETICS IN MEDICINE

IF6.2

2025-03-01

PREAI

Qebibo, Leila; Davakan, Amael; Nesson-Dauphin, Mathilde; Boulali, Najlae; Siquier-Pernet, Karine; Afenjar, Alexandra; Amiel, Jeanne; Bartholdi, Deborah; Barth, Magalie; Blondiaux, Eleonore; Cristian, Ingrid; Frazier, Zoe; Goldenberg, Alice; Good, Jean-Marc; Salussolia, Catherine Lourdes; Sahin, Mustafa; McCullagh, Helen; McDonald, Kimberly; McRae, Anne; Morrison, Jennifer; Pinner, Jason; Shinawi, Marwan; Toutain, Annick; Vyhnalkova, Emilie; Wheeler, Patricia G.; Wilnai, Yael; Hausman-Kedem, Moran; Coolen, Marion; Cantagrel, Vincent; Burglen, Lydie; Lory, Philippe

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Biallelic EPB41L3 variants underlie a developmental disorder with seizures and myelination defects

BRAIN

IF11.7

2024-09-18

PREAI

Werren, Elizabeth A.; Bey, Guillermo Rodriguez; Majethia, Purvi; Kaur, Parneet; Patil, Siddaramappa J.; Kekatpure, Minal, V; Afenjar, Alexandra; Qebibo, Leila; Burglen, Lydie; Tomoum, Hoda; Demurger, Florence; Duborg, Christele; Siddiqui, Shahyan; Tsan, Yao-Chang; Abdullah, Uzma; Ali, Zafar; Saadi, Saadia Maryam; Baig, Shahid Mahmood; Houlden, Henry; Maroofian, Reza; Padiath, Quasar Saleem; Bielas, Stephanie L.; Shukla, Anju

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Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders

MOVEMENT DISORDERS

IF7.6

2024-06-20

OAAI

Ortigoza-Escobar, Juan Dario; Zamani, Mina; Dorison, Nathalie; Sadeghian, Saeid; Azizimalamiri, Reza; Alvi, Javeria Raza; Sultan, Tipu; Galehdari, Hamid; Shariati, Gholamreza; Saberi, Alihossein; Leeuwen, Lisette; Zifarelli, Giovanni; Bauer, Peter; d'Hardemare, Vincent; Doummar, Diane; Roze, Emmanuel; Travaglini, Lorena; Nicita, Francesco; Ojea Ponce, Nuria; Zahraei, Seyed Mohammadsaleh; Alabdi, Lama; Tamim, Abdullah; Hashem, Mais O.; Ababneh, Faroug; Morrow, Michelle M.; Curry, Cynthia; Tam, Allison; Ruedy, Jessica; Bhambhani, Vikas; Veith, Regan; Stromme, Petter; Efthymiou, Stephanie; Alkuraya, Fowzan S.; Moreno-De-Luca, Andres; Burglen, Lydie; Houlden, Henry; Maroofian, Reza

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An autosomal-dominant childhood-onset disorder associated with pathogenic variants in VCP

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2023-11-01

OAAI

Mah-Som, Annelise Y.; Daw, Jil; Huynh, Diana; Wu, Mengcheng; Creekmore, Benjamin C.; Burns, William; Skinner, Steven A.; Holla, Oystein L.; Smeland, Marie F.; Planes, Marc; Uguen, Kevin; Redon, Sylvia; Bierhals, Tatjana; Scholz, Tasja; Denecke, Jonas; Mensah, Martin A.; Sczakiel, Henrike L.; Tichy, Heidelis; Verheyen, Sarah; Blatterer, Jasmin; Schreiner, Elisabeth; Thies, Jenny; Lam, Christina; Spaeth, Christine G.; Pena, Loren; Ramsey, Keri; Narayanan, Vinodh; Seaver, Laurie H.; Rodriguez, Diana; Afenjar, Alexandra; Burglen, Lydie; Lee, Edward B.; Chou, Tsui-Fen; Weihl, Conrad C.; Shinawi, Marwan S.

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TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions

BRAIN

IF11.7

2023-09-15

PREAI

Almousa, Hashem; Lewis, Sara A.; Bakhtiari, Somayeh; Nordlie, Sandra Hinz; Pagnozzi, Alex; Magee, Helen; Efthymiou, Stephanie; Heim, Jennifer A.; Cornejo, Patricia; Zaki, Maha S.; Anwar, Najwa; Maqbool, Shazia; Rahman, Fatima; Neilson, Derek E.; Vemuri, Anusha; Jin, Sheng Chih; Yang, Xiao-Ru; Heidari, Abolfazl; van Gassen, Koen; Trimouille, Aurelien; Thauvin-Robinet, Christel; Liu, James; Bruel, Ange-Line; Tomoum, Hoda; Shata, Mennatallah O.; Hashem, Mais O.; Toosi, Mehran Beiraghi; Karimiani, Ehsan Ghayoor; Yesil, Gozde; Lingappa, Lokesh; Baruah, Debangana; Ebrahimzadeh, Farnoosh; Van-Gils, Julien; Faivre, Laurence; Zamani, Mina; Galehdari, Hamid; Sadeghian, Saeid; Shariati, Gholamreza; Mohammad, Rahema; van der Smagt, Jasper; Qari, Alya; Vincent, John B.; Innes, A. Micheil; Dursun, Ali; Ozgul, R. Koksal; Akar, Halil Tuna; Bilguvar, Kaya; Mignot, Cyril; Keren, Boris; Raveli, Claudia; Burglen, Lydie; Afenjar, Alexandra; Kaat, Laura Donker; van Slegtenhorst, Marjon; Alkuraya, Fowzan; Houlden, Henry; Padilla-Lopez, Sergio; Maroofian, Reza; Sacher, Michael; Kruer, Michael C.

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Autosomal Dominant MPAN: Mosaicism Expands the Clinical Spectrum to Atypical Late-Onset Phenotypes

MOVEMENT DISORDERS

IF7.6

2023-08-21

OAAI

Angelini, Chloe; Durand, Christelle Marie; Fergelot, Patricia; Deforges, Julie; Vital, Anne; Menegon, Patrice; Sarrazin, Elizabeth; Bellance, Remi; Mathis, Stephane; Gonzalez, Victoria; Renaud, Mathilde; Frismand, Solene; Schmitt, Emmanuelle; Rouanet, Marie; Burglen, Lydie; Chabrol, Brigitte; Desnous, Beatrice; Arveiler, Benoit; Stevanin, Giovanni; Coupry, Isabelle; Goizet, Cyril

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Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders

BRAIN

IF11.7

2023-07-30

OAAI

Maroofian, Reza; Kaiyrzhanov, Rauan; Cali, Elisa; Zamani, Mina; Zaki, Maha S.; Ferla, Matteo; Tortora, Domenico; Sadeghian, Saeid; Saadi, Saadia Maryam; Abdullah, Uzma; Karimiani, Ehsan Ghayoor; Efthymiou, Stephanie; Yesil, Goezde; Alavi, Shahryar; Al Shamsi, Aisha M.; Tajsharghi, Homa; Abdel-Hamid, Mohamed S.; Saadi, Nebal Waill; Al Mutairi, Fuad; Alabdi, Lama; Beetz, Christian; Ali, Zafar; Toosi, Mehran Beiraghi; Rudnik-Schoeneborn, Sabine; Babaei, Meisam; Isohanni, Pirjo; Muhammad, Jameel; Khan, Sheraz; Al Shalan, Maha; Hickey, Scott E.; Marom, Daphna; Elhanan, Emil; Kurian, Manju A.; Marafi, Dana; Saberi, Alihossein; Hamid, Mohammad; Spaull, Robert; Meng, Linyan; Lalani, Seema; Maqbool, Shazia; Rahman, Fatima; Seeger, Juergen; Palculict, Timothy Blake; Lau, Tracy; Murphy, David; Mencacci, Niccolo Emanuele; Steindl, Katharina; Begemann, Anais; Rauch, Anita; Akbas, Sinan; Aslanger, Ayca Dilruba; Salpietro, Vincenzo; Yousaf, Hammad; Ben-Shachar, Shay; Ejeskaer, Katarina; Al Aqeel, Aida, I; High, Frances A.; Armstrong-Javors, Amy E.; Zahraei, Seyed Mohammadsaleh; Seifi, Tahereh; Zeighami, Jawaher; Shariati, Gholamreza; Sedaghat, Alireza; Asl, Samaneh Noroozi; Shahrooei, Mohmmad; Zifarelli, Giovanni; Burglen, Lydie; Ravelli, Claudia; Zschocke, Johannes; Schatz, Ulrich A.; Ghavideldarestani, Maryam; Kamel, Walaa A.; Van Esch, Hilde; Hackenberg, Annette; Taylor, Jenny C.; Al-Gazali, Lihadh; Bauer, Peter; Gleeson, Joseph J.; Alkuraya, Fowzan Sami; Lupski, James R.; Galehdari, Hamid; Azizimalamiri, Reza; Chung, Wendy K.; Baig, Shahid Mahmood; Houlden, Henry; Severino, Mariasavina

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EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2023-06-21

PREAI

Engel, Camille; Valence, Stephanie; Delplancq, Geoffroy; Maroofian, Reza; Accogli, Andrea; Agolini, Emanuele; Alkuraya, Fowzan S.; Baglioni, Valentina; Bagnasco, Irene; Becmeur-Lefebvre, Mathilde; Bertini, Enrico; Borggraefe, Ingo; Brischoux-Boucher, Elise; Bruel, Ange-Line; Brusco, Alfredo; Bubshait, Dalal K.; Cabrol, Christelle; Cilio, Maria Roberta; Cornet, Marie-Coralie; Coubes, Christine; Danhaive, Olivier; Delague, Valerie; Denomme-Pichon, Anne-Sophie; Di Giacomo, Marilena Carmela; Doco-Fenzy, Martine; Engels, Hartmut; Cremer, Kirsten; Gerard, Marion; Gleeson, Joseph G.; Heron, Delphine; Goffeney, Joanna; Guimier, Anne; Harms, Frederike L.; Houlden, Henry; Iacomino, Michele; Kaiyrzhanov, Rauan; Kamien, Benjamin; Karimiani, Ehsan Ghayoor; Kraus, Dror; Kuentz, Paul; Kutsche, Kerstin; Lederer, Damien; Massingham, Lauren; Mignot, Cyril; Morris-Rosendahl, Deborah; Nagarajan, Lakshmi; Odent, Sylvie; Ormieres, Clothilde; Partlow, Jennifer Neil; Pasquier, Laurent; Penney, Lynette; Philippe, Christophe; Piccolo, Gianluca; Poulton, Cathryn; Putoux, Audrey; Rio, Marlene; Rougeot, Christelle; Salpietro, Vincenzo; Scheffer, Ingrid; Schneider, Amy; Srivastava, Siddharth; Straussberg, Rachel; Striano, Pasquale; Valente, Enza Maria; Venot, Perrine; Villard, Laurent; Vitobello, Antonio; Wagner, Johanna; Wagner, Matias; Zaki, Maha S.; Zara, Federizo; Lesca, Gaetan; Yassaee, Vahid Reza; Miryounesi, Mohammad; Hashemi-Gorji, Farzad; Beiraghi, Mehran; Ashrafzadeh, Farah; Galehdari, Hamid; Walsh, Christopher; Novelli, Antonio; Tacke, Moritz; Sadykova, Dinara; Maidyrov, Yerdan; Koneev, Kairgali; Shashkin, Chingiz; Capra, Valeria; Zamani, Mina; Van Maldergem, Lionel; Burglen, Lydie; Piard, Juliette

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Author Correction: Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects (vol 14, 3403, 2023)

NATURE COMMUNICATIONS

IF15.7

2023-06-15

OAAI

Ayers, Katie L.; Eggers, Stefanie; Rollo, Ben N.; Smith, Katherine R.; Davidson, Nadia M.; Siddall, Nicole A.; Zhao, Liang; Bowles, Josephine; Weiss, Karin; Zanni, Ginevra; Burglen, Lydie; Ben-Shachar, Shay; Rosensaft, Jenny; Raas-Rothschild, Annick; Jorgensen, Anne; Schittenhelm, Ralf B.; Huang, Cheng; Robevska, Gorjana; van den Bergen, Jocelyn; Casagranda, Franca; Cyza, Justyna; Pachernegg, Svenja; Wright, David K.; Bahlo, Melanie; Oshlack, Alicia; O'Brien, Terrence J.; Kwan, Patrick; Koopman, Peter; Hime, Gary R.; Girard, Nadine; Hoffmann, Chen; Shilon, Yuval; Zung, Amnon; Bertini, Enrico; Milh, Mathieu; Ben Rhouma, Bochra; Belguith, Neila; Bashamboo, Anu; McElreavey, Kenneth; Banne, Ehud; Weintrob, Naomi; BenZeev, Bruria; Sinclair, Andrew H.

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Variants in SART3 cause a spliceosomopathy characterised by failure of testis development and neuronal defects

NATURE COMMUNICATIONS

IF15.7

2023-06-09

OAAI

Ayers, Katie L.; Eggers, Stefanie; Rollo, Ben N.; Smith, Katherine R.; Davidson, Nadia M.; Siddall, Nicole A.; Zhao, Liang; Bowles, Josephine; Weiss, Karin; Zanni, Ginevra; Burglen, Lydie; Ben-Shachar, Shay; Rosensaft, Jenny; Raas-Rothschild, Annick; Jorgensen, Anne; Schittenhelm, Ralf B.; Huang, Cheng; Robevska, Gorjana; van den Bergen, Jocelyn; Casagranda, Franca; Cyza, Justyna; Pachernegg, Svenja; Wright, David K.; Bahlo, Melanie; Oshlack, Alicia; O'Brien, Terrence J.; Kwan, Patrick; Koopman, Peter; Hime, Gary R.; Girard, Nadine; Hoffmann, Chen; Shilon, Yuval; Zung, Amnon; Bertini, Enrico; Milh, Mathieu; Ben Rhouma, Bochra; Belguith, Neila; Bashamboo, Anu; MacElreavey, Kenneth; Banne, Ehud; Weintrob, Naomi; BenZeev, Bruria; Sinclair, Andrew H.

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Spectrum of brain malformations in fetuses with mild tubulinopathy

ULTRASOUND IN OBSTETRICS & GYNECOLOGY

IF6.3

2023-06-02

OAAI

Hagege, R.; Haratz, K. Krajden; Malinger, G.; Ben-Sira, L.; Leibovitz, Z.; Heron, D.; Burglen, L.; Birnbaum, R.; Valence, S.; Keren, B.; Blumkin, L.; Jouannic, J. -m.; Lerman-Sagie, T.; Garel, C.

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Research Directions