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Transmitter concentration profiles in the synaptic cleft: an analytical model of release and diffusion

Biophysical journal, 1996-11, Vol.71 (5), p.2413-2426

1996

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Pattern Generation by Two Coupled Time-Discrete Neural Networks with Synaptic Depression

Neural computation, 1998-07, Vol.10 (5), p.1251-1275

1998

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Size principle and information theory

Biological cybernetics, 1997-01, Vol.76 (1), p.11-22

1997

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Structural and physiological properties of connections between individual reticulospinal axons and lumbar motoneurons of the frog

Journal of comparative neurology (1911), 2001-02, Vol.430 (4), p.433-447

2001

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Molekulare Autopsie nach plötzlichem Herztod: Ergänzende Untersuchungen nach unauffälligen Sektionsbefunden

Rechtsmedizin (Berlin, Germany), 2018-08, Vol.28 (4), p.317-329

2018

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Delineating MT-ATP6 -associated disease: From isolated neuropathy to early onset neurodegeneration

Neurology. Genetics, 2020-02, Vol.6 (1), p.e393-e393

2020

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene

Annals of neurology, 1998-10, Vol.44 (4), p.635-640

1998

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Respiratory chain deficiency in nonmitochondrial disease

Neurology. Genetics, 2015-06, Vol.1 (1), p.e6-e6

2015

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A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy

Journal of medical genetics, 1998-11, Vol.35 (11), p.895-900

1998

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Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

Journal of medical genetics, 2001-10, Vol.38 (10), p.665-673

2001

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Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR

Human genetics, 1997-10, Vol.100 (5-6), p.643-650

1997

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Problems in detecting mosaic DNA methylation in Angelman syndrome

European journal of human genetics : EJHG, 2003-12, Vol.11 (12), p.913-915

2003

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Reconstruction and subsurface lattice distortions in the (2 × 1)O-Ni(110) structure: A LEED analysis

Surface science, 1990, Vol.225 (1), p.171-183

1990

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Structure determination of an adsorbate-induced multilayer reconstruction: (1×2)-H/Ni(110)

Physical review letters, 1987-01, Vol.58 (2), p.148-151

1987

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Mechanistic and energetic aspects of the H-induced (1×2) reconstructed structures on Ni(110) and Pd(110)

Surface science, 1987-10, Vol.189, p.177-184

1987

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNAser(UCN) gene

Annals of neurology, 1998-10, Vol.44 (4), p.635-640

1998

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A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNASer(UCN) mutations in a subgroup with syndromal encephalopathy

Journal of medical genetics, 1998, Vol.35 (11), p.895-900

1998

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Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblasts

Enzyme & protein, 1996, Vol.49 (5-6), p.321

1996

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Summary Abstract: Strong vertical intralayer distortions as a key structural feature in the (1×2)H reconstructed Ni(110) surface

Journal of vacuum science & technology. A, Vacuum, surfaces, and films, 1987-07, Vol.5 (4), p.793-794

1987

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Transmitter concentration profiles in the synaptic cleft: an analytical model of release and diffusion

Pattern Generation by Two Coupled Time-Discrete Neural Networks with Synaptic Depression

Size principle and information theory

Structural and physiological properties of connections between individual reticulospinal axons and lumbar motoneurons of the frog

Maternal variants in NLRP and other maternal effect proteins are associated with multilocus imprinting disturbance in offspring

Molekulare Autopsie nach plötzlichem Herztod: Ergänzende Untersuchungen nach unauffälligen Sektionsbefunden

Delineating MT-ATP6 -associated disease: From isolated neuropathy to early onset neurodegeneration

Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene

Respiratory chain deficiency in nonmitochondrial disease

A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy

Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies

Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR

Problems in detecting mosaic DNA methylation in Angelman syndrome

Reconstruction and subsurface lattice distortions in the (2 × 1)O-Ni(110) structure: A LEED analysis

Structure determination of an adsorbate-induced multilayer reconstruction: (1×2)-H/Ni(110)

Mechanistic and energetic aspects of the H-induced (1×2) reconstructed structures on Ni(110) and Pd(110)

Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNAser(UCN) gene

A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNASer(UCN) mutations in a subgroup with syndromal encephalopathy

Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblasts

Summary Abstract: Strong vertical intralayer distortions as a key structural feature in the (1×2)H reconstructed Ni(110) surface

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