Kaindl AM - Search Results

1

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.

Weiß C, Ziegler A, Becker LL, Johannsen J, Brennenstuhl H, Schreiber G, Flotats-Bastardas M, Stoltenburg C, Hartmann H, Illsinger S, Denecke J, Pechmann A, Müller-Felber W, Vill K, Blaschek A, Smitka M, van der Stam L, Weiss K, Winter B, Goldhahn K, Plecko B, Horber V, Bernert G, Husain RA, Rauscher C, Trollmann R, Garbade SF, Hahn A, von der Hagen M, Kaindl AM. Weiß C, et al. Among authors: kaindl am. Lancet Child Adolesc Health. 2022 Jan;6(1):17-27. doi: 10.1016/S2352-4642(21)00287-X. Epub 2021 Oct 29. Lancet Child Adolesc Health. 2022. PMID: 34756190

2

Limb girdle muscular dystrophy type 2I caused by a novel missense mutation in the FKRP gene presenting as acute virus-associated myositis in infancy.

von der Hagen M, Kaindl AM, Koehler K, Mitzscherling P, Häusler HJ, Stoltenburg-Didinger G, Huebner A. von der Hagen M, et al. Among authors: kaindl am. Eur J Pediatr. 2006 Jan;165(1):62-3. doi: 10.1007/s00431-005-1752-6. Epub 2005 Sep 6. Eur J Pediatr. 2006. PMID: 16143867 No abstract available.

3

Selenoprotein N muscular dystrophy: differential diagnosis for early-onset limited mobility of the spine.

Sponholz S, von der Hagen M, Hahn G, Seifert J, Richard P, Stoltenburg-Didinger G, Ferreiro A, Kaindl AM. Sponholz S, et al. Among authors: kaindl am. J Child Neurol. 2006 Apr;21(4):316-20. doi: 10.1177/08830738060210041401. J Child Neurol. 2006. PMID: 16900928

4

Spinal muscular atrophy with respiratory distress type 1 (SMARD1).

Kaindl AM, Guenther UP, Rudnik-Schöneborn S, Varon R, Zerres K, Schuelke M, Hübner C, von Au K. Kaindl AM, et al. J Child Neurol. 2008 Feb;23(2):199-204. doi: 10.1177/0883073807310989. J Child Neurol. 2008. PMID: 18263757

5

Sedative and anticonvulsant drugs suppress postnatal neurogenesis.

Stefovska VG, Uckermann O, Czuczwar M, Smitka M, Czuczwar P, Kis J, Kaindl AM, Turski L, Turski WA, Ikonomidou C. Stefovska VG, et al. Among authors: kaindl am. Ann Neurol. 2008 Oct;64(4):434-45. doi: 10.1002/ana.21463. Ann Neurol. 2008. PMID: 18991352

6

Growth and psychomotor development of patients with Duchenne muscular dystrophy.

Sarrazin E, von der Hagen M, Schara U, von Au K, Kaindl AM. Sarrazin E, et al. Among authors: kaindl am. Eur J Paediatr Neurol. 2014 Jan;18(1):38-44. doi: 10.1016/j.ejpn.2013.08.008. Epub 2013 Sep 25. Eur J Paediatr Neurol. 2014. PMID: 24100172

7

Diagnostic approach to microcephaly in childhood: a two-center study and review of the literature.

von der Hagen M, Pivarcsi M, Liebe J, von Bernuth H, Didonato N, Hennermann JB, Bührer C, Wieczorek D, Kaindl AM. von der Hagen M, et al. Among authors: kaindl am. Dev Med Child Neurol. 2014 Aug;56(8):732-41. doi: 10.1111/dmcn.12425. Epub 2014 Mar 12. Dev Med Child Neurol. 2014. PMID: 24617602 Free article. Review.

8

Altered inhibition and excitation in neocortical circuits in congenital microcephaly.

Zaqout S, Blaesius K, Wu YJ, Ott S, Kraemer N, Becker LL, Rosário M, Rosenmund C, Strauss U, Kaindl AM. Zaqout S, et al. Among authors: kaindl am. Neurobiol Dis. 2019 Sep;129:130-143. doi: 10.1016/j.nbd.2019.05.008. Epub 2019 May 15. Neurobiol Dis. 2019. PMID: 31102767

9

Just Expect It: Compound Heterozygous Variants of POMT1 in a Consanguineous Family-The Role of Next Generation Sequencing in Neuromuscular Disorders.

von der Hagen M, Becker LL, Wienker TF, Smitka M, Musante L, Ropers HH, Huebner A, Hu H, Kaindl AM. von der Hagen M, et al. Among authors: kaindl am. Neuropediatrics. 2020 Feb;51(1):72-75. doi: 10.1055/s-0039-1695787. Epub 2019 Oct 18. Neuropediatrics. 2020. PMID: 31627234

10

Clinical and Magnetic Resonance Imaging Outcome Predictors in Pediatric Anti-N-Methyl-D-Aspartate Receptor Encephalitis.

Bartels F, Krohn S, Nikolaus M, Johannsen J, Wickström R, Schimmel M, Häusler M, Berger A, Breu M, Blankenburg M, Stoffels J, Hendricks O, Bernert G, Kurlemann G, Knierim E, Kaindl A, Rostásy K, Finke C. Bartels F, et al. Ann Neurol. 2020 Jul;88(1):148-159. doi: 10.1002/ana.25754. Epub 2020 May 29. Ann Neurol. 2020. PMID: 32314416

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