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Peptide structural analysis by solid-state NMR spectroscopy

BIOPOLYM, 1999, Vol.51 (3), p.174-190

1999

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Alignment of Lysine-Anchored Membrane Peptides under Conditions of Hydrophobic Mismatch: A CD, 15N and 31P Solid-State NMR Spectroscopy Investigation

Biochemistry (Easton), 2000-10, Vol.39 (43), p.13106-13114

2000

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Attached and Suspended Denitrifier Communities in Pristine Limestone Aquifers Harbor High Fractions of Potential Autotrophs Oxidizing Reduced Iron and Sulfur Compounds

Microbial ecology, 2017-08, Vol.74 (2), p.264-277

2017

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Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study

The Lancet (British edition), 2005-11, Vol.366 (9499), p.1794-1796

2005

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NPC1: Complete genomic sequence, mutation analysis, and characterization of haplotypes

Human mutation, 2002-01, Vol.19 (1), p.30-38

2002

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Gene therapy: prospects for glycolipid storage diseases

Philosophical transactions of the Royal Society of London. Series B. Biological sciences, 2003-05, Vol.358 (1433), p.921-925

2003

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Long-term expression and transfer of arylsulfatase A into brain of arylsulfatase A-deficient mice transplanted with bone marrow expressing the arylsulfatase A cDNA from a retroviral vector

Gene therapy, 2000-07, Vol.7 (14), p.1250-1257

2000

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Clinical findings in Niemann-Pick disease type B

Internal medicine journal, 2006-02, Vol.36 (2), p.135-136

2006

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Efficacy of a two-component acellular pertussis vaccine in infants

The Pediatric infectious disease journal, 1997-11, Vol.16 (11), p.1038-1044

1997

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Effects of 28-day mechanical and chewing stress on content of bound and diffusible ions in muscles of mastication

Experimental and toxicologic pathology : official journal of the Gesellschaft für Toxikologische Pathologie, 2001-06, Vol.53 (2-3), p.207-213

2001

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Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological study

European journal of pediatrics, 1991-06, Vol.150 (8), p.584-591

1991

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Neuraminidase assay in cultured human fibroblasts: in situ versus in vitro procedures

Clinica chimica acta, 1996-07, Vol.251 (2), p.163-171

1996

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Vitamin K1 content of maternal milk: influence of the stage of lactation, lipid composition, and vitamin K1 supplements given to the mother

Pediatric research, 1987-11, Vol.22 (5), p.513-517

1987

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Ultrasound echogenic splenic tumors: nodular manifestation of type C Niemann-Pick disease

Ultraschall in der Medizin, 1990-06, Vol.11 (3), p.119-122

1990

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Metachromatic reaction of pseudoisocyanine with sulfatides in metachromatic leukodystrophy (MLD). I. Technique of histochemical staining

Acta neuropathologica, 1974-02, Vol.27 (2), p.177-180

1974

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Neurovisceral lipidosis compatible with Niemann-Pick disease type C: morphological and biochemical studies of a late infantile case and enzyme and lipid assays in a prenatal case of the same family

Acta neuropathologica, 1978-01, Vol.43 (1-2), p.97-104

1978

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Clinical and histological diagnosis of a case of familial adult metachromatic leucodystrophy (author's transl)

Journal of neurology, 1974, Vol.207 (3), p.189-204

1974

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Letters: A simple sphingomyelinase determination for Niemann-Pick disease: differential diagnosis of types A, B and C

Journal of neurochemistry, 1973-10, Vol.21 (4), p.999-1001

1973

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Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase B

Neuropädiatrie, 1980-05, Vol.11 (2), p.161-175

1980

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Prenatal diagnosis of globoid-cell leukodystrophy (Krabbe's disease) (author's transl)

Deutsche medizinische Wochenschrift, 1976-05, Vol.101 (21), p.821

1976

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Metachromatic leucodystrophy. A genetic study of a familial adult form of metachromatic leucodystrophy (author's transl)

Archiv fur Psychiatrie und Nervenkrankheiten, 1974, Vol.219 (4), p.369

1974

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Niemann-Pick disease type B: An enzymatically confirmed case with unexpected retinal involvement (author's transl)

Albrecht von Graefes Archiv für klinische und experimentale Ophthalmologie, 1978-05, Vol.206 (2), p.79-88

1978

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Peptide structural analysis by solid-state NMR spectroscopy

Alignment of Lysine-Anchored Membrane Peptides under Conditions of Hydrophobic Mismatch: A CD, 15N and 31P Solid-State NMR Spectroscopy Investigation

Attached and Suspended Denitrifier Communities in Pristine Limestone Aquifers Harbor High Fractions of Potential Autotrophs Oxidizing Reduced Iron and Sulfur Compounds

Prevalence of Fabry disease in patients with cryptogenic stroke: a prospective study

NPC1: Complete genomic sequence, mutation analysis, and characterization of haplotypes

Gene therapy: prospects for glycolipid storage diseases

Long-term expression and transfer of arylsulfatase A into brain of arylsulfatase A-deficient mice transplanted with bone marrow expressing the arylsulfatase A cDNA from a retroviral vector

Clinical findings in Niemann-Pick disease type B

Efficacy of a two-component acellular pertussis vaccine in infants

Effects of 28-day mechanical and chewing stress on content of bound and diffusible ions in muscles of mastication

Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological study

Neuraminidase assay in cultured human fibroblasts: in situ versus in vitro procedures

Vitamin K1 content of maternal milk: influence of the stage of lactation, lipid composition, and vitamin K1 supplements given to the mother

Ultrasound echogenic splenic tumors: nodular manifestation of type C Niemann-Pick disease

Metachromatic reaction of pseudoisocyanine with sulfatides in metachromatic leukodystrophy (MLD). I. Technique of histochemical staining

Neurovisceral lipidosis compatible with Niemann-Pick disease type C: morphological and biochemical studies of a late infantile case and enzyme and lipid assays in a prenatal case of the same family

Clinical and histological diagnosis of a case of familial adult metachromatic leucodystrophy (author's transl)

Letters: A simple sphingomyelinase determination for Niemann-Pick disease: differential diagnosis of types A, B and C

Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase B

Prenatal diagnosis of globoid-cell leukodystrophy (Krabbe's disease) (author's transl)

Metachromatic leucodystrophy. A genetic study of a familial adult form of metachromatic leucodystrophy (author's transl)

Niemann-Pick disease type B: An enzymatically confirmed case with unexpected retinal involvement (author's transl)

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