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External quality assessment (EQA) of Neisseria gonorrhoeae antimicrobial susceptibility testing in primary laboratories in Germany

BMC infectious diseases, 2020-07, Vol.20 (1), p.1-514, Article 514

2020

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Rapid Second-Tier Molecular Genetic Analysis for Congenital Adrenal Hyperplasia Attributable to Steroid 21-Hydroxylase Deficiency

Clinical chemistry (Baltimore, Md.), 2005-02, Vol.51 (2), p.298-304

2005

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Brain aluminum, magnesium and phosphorus contents of control and Alzheimer-diseased patients

Journal of Alzheimer's disease, 2005-08, Vol.7 (4), p.273

2005

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Correlation of HPV16 L1 Capsid Protein Expression in Cervical Dysplasia with HPV16 DNA Concentration, HPV16 E6I mRNA and Histologic Outcome

Acta cytologica, 2009-07, Vol.53 (4), p.396-401

2009

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Microglia and the Development of Spongiform Change in Creutzfeldt-Jakob Disease

Journal of neuropathology and experimental neurology, 1998-03, Vol.57 (3), p.246-256

1998

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Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease

Neurogenetics, 1998-03, Vol.1 (3), p.197-204

1998

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On the question of apoptosis in the Parkinsonian substantia nigra

Acta neuropathologica, 1997-02, Vol.93 (2), p.105-108

1997

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Unexplained DNA melting behavior in a genotyping assay

Clinical chemistry (Baltimore, Md.), 2002, Vol.48 (1), p.199-201

2002

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Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain

Acta neuropathologica, 1997-12, Vol.94 (6), p.532-538

1997

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Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 2I-hydroxylase deficiency

Clinical chemistry (Baltimore, Md.), 2005-02, Vol.51 (2), p.298

2005

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Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease

Neurogenetics, 1999-04, Vol.2 (2), p.121-127

1999

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Microglial Activation in Alzheimer Disease: Association with APOE Genotype

Brain pathology (Zurich, Switzerland), 1998-07, Vol.8 (3), p.439-447

1998

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Role of Mitochondria in Parkinson Disease

Biological chemistry, 1999-07, Vol.380 (7-8), p.865-870

1999

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Type-Specific Detection of Human Papillomaviruses in a Routine Laboratory Setting – Improved Sensitivity and Specificity of PCR and Sequence Analysis Compared to Direct Hybridisation

Clinical chemistry and laboratory medicine, 2003-06, Vol.41 (6), p.787-791

2003

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Genotype-Phenotype Correlation in Gemistocytic Astrocytomas

Neurosurgery, 2001-01, Vol.48 (1), p.187-194

2001

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Determination of strontium and its relation to other alkaline earth elements in human brain samples

Microchemical journal, 2005, Vol.79 (1), p.375-381

2005

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Genotype-phenotype correlation in gemistocytic astrocytomas

Neurosurgery, 2001-01, Vol.48 (1), p.187-194

2001

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Non-Radioactive Direct Sequencing of PCR Products Amplified from Neuropathological Specimens

Brain pathology (Zurich, Switzerland), 1993-10, Vol.3 (4), p.421-424

1993

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Neurodegeneration and aging: Role of the second genome

Journal of neuroscience research, 1998-04, Vol.52 (1), p.1-6

1998

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Nonradioactive PCR sequencing using digoxigenin

Methods in molecular biology (Clifton, N.J.), 2003, Vol.226, p.347

2003

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The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction

Movement disorders, 1997-09, Vol.12 (5), p.639-645

1997

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Association between ACT polymorphism and Alzheimer's disease

Neurology, 1998-02, Vol.50 (2), p.575

1998

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Genotype-phenotype correlation in gemistocytic astrocytomas. Commentaries

Neurosurgery, 2001, Vol.48 (1), p.187-194

2001

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Genotyp-Analyse bei Hirnerkrankungen

Neuroforum, 1996-08, Vol.2 (3), p.11-21

1996

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Chapter 22 A new approach to the genetic analysis of nervous system diseases: Retrospective genotyping of archival brains

Progress in Brain Research, 1998, Vol.117, p.307-313

1998

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External quality assessment (EQA) of Neisseria gonorrhoeae antimicrobial susceptibility testing in primary laboratories in Germany

Rapid Second-Tier Molecular Genetic Analysis for Congenital Adrenal Hyperplasia Attributable to Steroid 21-Hydroxylase Deficiency

Brain aluminum, magnesium and phosphorus contents of control and Alzheimer-diseased patients

Correlation of HPV16 L1 Capsid Protein Expression in Cervical Dysplasia with HPV16 DNA Concentration, HPV16 E6I mRNA and Histologic Outcome

Microglia and the Development of Spongiform Change in Creutzfeldt-Jakob Disease

Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease

On the question of apoptosis in the Parkinsonian substantia nigra

Unexplained DNA melting behavior in a genotyping assay

Long-lasting perivascular accumulation of major histocompatibility complex class II-positive lipophages in the spinal cord of stroke patients: possible relevance for the immune privilege of the brain

Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 2I-hydroxylase deficiency

Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson disease

Microglial Activation in Alzheimer Disease: Association with APOE Genotype

Role of Mitochondria in Parkinson Disease

Type-Specific Detection of Human Papillomaviruses in a Routine Laboratory Setting – Improved Sensitivity and Specificity of PCR and Sequence Analysis Compared to Direct Hybridisation

Genotype-Phenotype Correlation in Gemistocytic Astrocytomas

Determination of strontium and its relation to other alkaline earth elements in human brain samples

Genotype-phenotype correlation in gemistocytic astrocytomas

Non-Radioactive Direct Sequencing of PCR Products Amplified from Neuropathological Specimens

Neurodegeneration and aging: Role of the second genome

Nonradioactive PCR sequencing using digoxigenin

The 'common deletion' is not increased in parkinsonian substantia nigra as shown by competitive polymerase chain reaction

Association between ACT polymorphism and Alzheimer's disease

Genotype-phenotype correlation in gemistocytic astrocytomas. Commentaries

Genotyp-Analyse bei Hirnerkrankungen

Chapter 22 A new approach to the genetic analysis of nervous system diseases: Retrospective genotyping of archival brains

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