Lena‐Luise Becker - Publications, H-index & Citations

Lena‐Luise Becker

Berlin Institute of Health

11H指数

39论文数

487被引数

收录论文 11

发表时间

Long-Term Efficacy and Safety of Mammalian Target of Rapamycin Inhibitor Treatment for Subependymal Giant Cell Astrocytoma in Tuberous Sclerosis 结节性硬化症中雷帕霉素靶蛋白抑制剂治疗室管膜下巨细胞星形细胞瘤的长期疗效与安全性

PEDIATRIC NEUROLOGY

IF2.1

2025-07-01

PREAI

Becker, Lena-Luise; Agricola, Karen; Ritter, David M.; Care, Marguerite M.; Krueger, Darcy A.; Franz, David Neal

Phenotype Spectrum of TRPM3-Associated Disorders

ANNALS OF NEUROLOGY

IF7.7

2025-01-03

OAAI

Jolitz, Laura; Helbig, Ingo; Fitzgerald, Mark P.; McKeown Ruggiero, Sarah; Cohen, Stacey; Angelini, Chloe; Vallespin, Elena; Michaud, Vincent; Gerasimenko, Anna; Cogne, Benjamin; Isidor, Bertrand; Keren, Boris; Dyment, David; Heron, Delphine; Karstensen, Helena Gasdal; Cuppen, Inge; Christodoulou, John; Wilson, Meredith; Lake, Nicole J.; Biskup, Saskia; Syrbe, Steffen; Mori, Takayasu; Becker, Lena-Luise; Kaindl, Angela M.

Mammalian Target of Rapamycin Inhibitor Levels Decrease Under Cenobamate Treatment

PEDIATRIC NEUROLOGY

IF2.1

2024-12-01

PREAI

Becker, Lena-Luise; Agricola, Karen; Ritter, David M.; Krueger, Darcy A.; Franz, David Neal

Efficacy fi cacy and safety of gene therapy with onasemnogene abeparvovec in children with spinal muscular atrophy in the D-A-CH-region: a population-based observational study

LANCET REGIONAL HEALTH-EUROPE

IF13

2024-12-01

OAAI

Weiss, Claudia; Becker, Lena-Luise; Friese, Johannes; Blaschek, Astrid; Hahn, Andreas; Illsinger, Sabine; Schwartz, Oliver; Bernert, Guenther; von der Hagen, Maja; Husain, Ralf A.; Goldhahn, Klaus; Kirschner, Janbernd; Pechmann, Astrid; Flotats-Bastardas, Marina; Schreiber, Gudrun; Schara, Ulrike; Plecko, Barbara; Trollmann, Regina; Horber, Veronka; Wilichowski, Ekkehard; Baumann, Matthias; Klein, Andrea; Eisenkoelbl, Astrid; Koehler, Cornelia; Stettner, Georg M.; Cirak, Sebahattin; Hasselmann, Oswald; Kaindl, Angela M.; Garbade, Sven F.; Johannsen, Jessika; Ziegler, Andreas

The expanding clinical and genetic spectrum of DYNC1H1-related disorders

BRAIN

IF11.7

2024-06-08

OAAI

Moeller, Birk; Becker, Lena-Luise; Saffari, Afshin; Afenjar, Alexandra; Coci, Emanuele G.; Williamson, Rachel; Ward-Melver, Catherine; Gibaud, Marc; Sedlackova, Lucie; Lassuthova, Petra; Liba, Zuzana; Vlckova, Marketa; William, Nancy; Klee, Eric W.; Gavrilova, Ralitza H.; Levy, Jonathan; Capri, Yline; Scavina, Mena; Koerner, Robert Walter; Valivullah, Zaheer; Weiss, Claudia; Moeller, Greta Marit; Frazier, Zoe; 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; Kuesters, Benno; Beggs, Alan H.; Sveden, Abigail; Chopra, Maya; Genetti, Casie A.; Nicolai, Joost; Doetsch, Joerg; Koy, Anne; Boennemann, Carsten G.; von der Hagen, Maja; von Kleist-Retzow, Juergen-Christoph; Voermans, Nicol C.; Jungbluth, Heinz; Dafsari, Hormos Salimi

Primidone improves symptoms in TRPM3-linked developmental and epileptic encephalopathy with spike-and-wave activation in sleep Primidone通过睡眠中的尖峰和波形激活改善TRPM3-linked发育性和癫痫性脑病的症状

EPILEPSIA

IF6.6

2023-03-28

OAAI

Becker, Lena-Luise; Horn, Denise; Boschann, Felix; Van Hoeymissen, Evelien; Voets, Thomas; Vriens, Joris; Prager, Christine; Kaindl, Angela M.

Monoallelic CRMP1 gene variants cause neurodevelopmental disorder 单等位基因CRMP1基因变异导致神经发育障碍

ELIFE

IF0

2022-12-13

OAAI

Ravindran, Ethiraj; Arashiki, Nobuto; Becker, Lena-Luise; Takizawa, Kohtaro; Levy, Jonathan; Rambaud, Thomas; Makridis, Konstantin L.; Goshima, Yoshio; Li, Na; Vreeburg, Maaike; Demeer, Benedicte; Dickmanns, Achim; Stegmann, Alexander P. A.; Hu, Hao; Nakamura, Fumio; Kaindl, Angela M.

Beware of Neurotoxins in Common Plants: Water Hemlock Poisoning Presenting as Convulsive Status Epilepticus

PEDIATRIC NEUROLOGY

IF2.1

2022-02-01

PREAI

Arsenova, Radina; Prager, Christine; Becker, Lena-Luise; Scholtis, Stefan; Methling, Maximilian; Kaindl, Angela M.

Gene replacement therapy with onasemnogene abeparvovec in children with spinal muscular atrophy aged 24 months or younger and bodyweight up to 15 kg: an observational cohort study

LANCET CHILD & ADOLESCENT HEALTH

IF15.5

2022-01-01

PREAI

Weiss, Claudia; Ziegler, Andreas; Becker, Lena-Luise; Johannsen, Jessika; Brennenstuhl, Heiko; Schreiber, Gudrun; Flotats-Bastardas, Marina; Stoltenburg, Corinna; Hartmann, Hans; Illsinger, Sabine; Denecke, Jonas; Pechmann, Astrid; Muller-Felber, Wolfgang; Vill, Katharina; Blaschek, Astrid; Smitka, Martin; van der Stam, Lieske; Weiss, Katja; Winter, Benedikt; Goldhahn, Klaus; Plecko, Barbara; Horber, Veronka; Bernert, Gunther; Husain, Ralf A.; Rauscher, Christian; Trollmann, Regina; Garbade, Sven F.; Hahn, Andreas; von der Hagen, Maja; Kaindl, Angela M.

Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders

HUMAN MOLECULAR GENETICS

IF3.2

2021-01-01

OAAI

Ravindran, Ethiraj; Juehlen, Ramona; Vieira-Vieira, Carlos H.; Thuong Ha; Salzberg, Yuval; Fichtman, Boris; Luise-Becker, Lena; Martins, Nuno; Picker-Minh, Sylvie; Bessa, Paraskevi; Arts, Peer; Jackson, Matilda R.; Taranath, Ajay; Kamien, Benjamin; Barnett, Christopher; Li, Na; Tarabykin, Victor; Stoltenburg-Didinger, Gisela; Harel, Amnon; Selbach, Matthias; Dickmanns, Achim; Fahrenkrog, Birthe; Hu, Hao; Scott, Hamish; Kaindl, Angela M.

Altered inhibition and excitation in neocortical circuits in congenital microcephaly

NEUROBIOLOGY OF DISEASE

IF5.6

2019-09-01

OAAI

Zaqout, Sami; Blaesius, Kathrin; Wu, Yuan-Ju; Ott, Stefanie; Kraemer, Nadine; Becker, Lena-Luise; Rosario, Marta; Rosenmund, Christian; Strauss, Ulf; Kaindl, Angela M.

研究方向