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1.
Spitzer, H. et al.: Interpretable surface-based detection of focal cortical dysplasias: A Multi-centre Epilepsy Lesion Detection study. Brain, DOI: 10.1093/brain/awac224 (2022)
2.
Stenton, S. et al.: DNAJC30 defect: A frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome. Brain 145, 1624-1631 (2022)
3.
Sundaram, S.M.* et al.: Gene therapy targeting the blood-brain barrier improves neurological symptoms in a model of genetic MCT8 deficiency. Brain, DOI: 10.1093/brain/awac243 (2022)
4.
Giesert, F.: c-Abl phosphorylation primes PARIS for neurodegeneration. Brain 144, 3555-3557 (2021)
5.
Invernizzi, F.* et al.: Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3. Brain 144:e74 (2021)
6.
Kaiyrzhanov, R.* et al.: Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum. Brain 144, e30 (2021)
7.
Macrini, C.* et al.: Features of MOG required for recognition by patients with MOG antibody-associated disorders. Brain 144, 2375-2389 (2021)
8.
Mirza-Schreiber, N. et al.: Blood DNA methylation provides an accurate biomarker of KMT2B-related dystonia and predicts onset. Brain, DOI: 10.1093/brain/awab360 (2021)
9.
Monfrini, E.* et al.: HOPS-associated neurological disorders (HOPSANDs): Linking endolysosomal dysfunction to the pathogenesis of dystonia. Brain 144, 2610-2615 (2021)
10.
Neuray, C.* et al.: Early-onset phenotype of bi-allelic GRN mutations. Brain 144:e22 (2021)
11.
Riedhammer, K.M.* et al.: De novo stop-loss variants in CLDN11 cause hypomyelinating leukodystrophy. Brain 144, 411-419 (2021)
12.
Zech, M. et al.: MATR3 haploinsufficiency and early-onset neurodegeneration. Brain 144:e72 (2021)
13.
Mak, C.C.Y.* et al.: MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain 143, 55-68 (2020)
14.
Zhou, J.* et al.: NAD(P)HX dehydratase (NAXD) deficiency: A novel neurodegenerative disorder exacerbated by febrile illnesses (vol 142, pg 50, 2019). Brain 143:e15 (2020)
15.
Zhou, J.* et al.: NAD(P)HX dehydratase (NAXD) deficiency: A novel neurodegenerative disorder exacerbated by febrile illnesses. Brain 143:e8 (2020)
16.
Esposito, A.* et al.: Biallelic DMXL2 mutations impair autophagy and cause Ohtahara syndrome with progressive course. Brain 142, 3876-3891 (2019)
17.
Forouhideh, Y.* et al.: A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification. Brain 142, e4 (2019)
18.
Van Bergen, N.J.* et al.: NAD(P)HX dehydratase (NAXD) deficiency: A novel neurodegenerative disorder exacerbated by febrile illnesses. Brain 142, 50-58 (2019)
19.
Vaz, F.M.* et al.: Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia. Brain 142, 3382-3397 (2019)
20.
Lessel, D.* et al.: BCL11B mutations in patients affected by a neurodevelopmental disorder with reduced type 2 innate lymphoid cells. Brain 141, 2299-2311 (2018)