Hahn G - Search Results

1

Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene.

Schmelzer L, Smitka M, Wolf C, Lucas N, Tüngler V, Hahn G, Tzschach A, Di Donato N, Lee-Kirsch MA, von der Hagen M. Schmelzer L, et al. Among authors: hahn g. Eur J Paediatr Neurol. 2018 Jan;22(1):186-189. doi: 10.1016/j.ejpn.2017.11.003. Epub 2017 Nov 22. Eur J Paediatr Neurol. 2018. PMID: 29221912

2

Acquired sensorimotor polyneuropathy in an adolescent boy with primary intracranial sarcoma.

Storch K, Schriever V, Hahn G, Sell K, Smitka M, Suttorp M, von der Hagen M, Schallner J. Storch K, et al. Among authors: hahn g. Eur J Paediatr Neurol. 2019 Jul;23(4):662-667. doi: 10.1016/j.ejpn.2019.04.005. Epub 2019 May 4. Eur J Paediatr Neurol. 2019. PMID: 31105004

3

Variable clinical course in acute necrotizing encephalopathy and identification of a novel RANBP2 mutation.

Sell K, Storch K, Hahn G, Lee-Kirsch MA, Ramantani G, Jackson S, Neilson D, von der Hagen M, Hehr U, Smitka M. Sell K, et al. Among authors: hahn g. Brain Dev. 2016 Sep;38(8):777-80. doi: 10.1016/j.braindev.2016.02.007. Epub 2016 Feb 26. Brain Dev. 2016. PMID: 26923722

4

Novel Mutation in the DKC1 Gene: Neonatal Hoyeraal-Hreidarsson Syndrome As a Rare Differential Diagnosis in Pontocerebellar Hypoplasia, Primary Microcephaly, and Progressive Bone Marrow Failure.

Dehmel M, Brenner S, Suttorp M, Hahn G, Schützle H, Dinger J, Di Donato N, Mackenroth L, von der Hagen M. Dehmel M, et al. Among authors: hahn g. Neuropediatrics. 2016 Jun;47(3):182-6. doi: 10.1055/s-0036-1578799. Epub 2016 Mar 7. Neuropediatrics. 2016. PMID: 26951492

5

Cerebellar atrophy on top of motor neuron compromise as indicator of late-onset GM2 gangliosidosis.

Hölzer HT, Boschann F, Hennermann JB, Hahn G, Hermann A, von der Hagen M, Tüngler V. Hölzer HT, et al. Among authors: hahn g. J Neurol. 2021 Jun;268(6):2259-2262. doi: 10.1007/s00415-021-10492-y. Epub 2021 Mar 9. J Neurol. 2021. PMID: 33751187 Free PMC article. No abstract available.

6

Unusual radiological presentation of tuberous sclerosis complex with leptomeningeal angiomatosis associated with a hypomorphic mutation in the TSC2 gene.

Ramantani G, Niggemann P, Hahn G, Näke A, Fahsold R, Lee-Kirsch MA. Ramantani G, et al. Among authors: hahn g. J Child Neurol. 2009 Mar;24(3):333-7. doi: 10.1177/0883073808323021. J Child Neurol. 2009. PMID: 19258292

7

Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?

Heinen A, Schnabel A, Brück N, Smitka M, Wolf C, Lucas N, Dollinger S, Hahn G, Günther C, Berner R, Lee-Kirsch MA, Schuetz C. Heinen A, et al. Among authors: hahn g. Rheumatology (Oxford). 2021 Apr 6;60(4):e136-e138. doi: 10.1093/rheumatology/keaa657. Rheumatology (Oxford). 2021. PMID: 33200187 No abstract available.

8

Childhood primary large vessel CNS vasculitis: single-centre experience and review of the literature.

Walsh S, Knöfler R, Hahn G, Lohse J, Berner R, Brenner S, Smitka M, von der Hagen M, Hedrich CM. Walsh S, et al. Among authors: hahn g. Clin Exp Rheumatol. 2017 Mar-Apr;35 Suppl 103(1):213-220. Epub 2017 Mar 28. Clin Exp Rheumatol. 2017. PMID: 28375836 Review.

9

Recurrent de novo BICD2 mutation associated with arthrogryposis multiplex congenita and bilateral perisylvian polymicrogyria.

Ravenscroft G, Di Donato N, Hahn G, Davis MR, Craven PD, Poke G, Neas KR, Neuhann TM, Dobyns WB, Laing NG. Ravenscroft G, et al. Among authors: hahn g. Neuromuscul Disord. 2016 Nov;26(11):744-748. doi: 10.1016/j.nmd.2016.09.009. Epub 2016 Sep 19. Neuromuscul Disord. 2016. PMID: 27751653

10

Clinical Perspective on Primary Angiitis of the Central Nervous System in Childhood (cPACNS).

Smitka M, Bruck N, Engellandt K, Hahn G, Knoefler R, von der Hagen M. Smitka M, et al. Among authors: hahn g. Front Pediatr. 2020 Jul 3;8:281. doi: 10.3389/fped.2020.00281. eCollection 2020. Front Pediatr. 2020. PMID: 32719754 Free PMC article. Review.

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