Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

K Harzer

Showing results (31-40 of 126) with videos related to

Pageof 13
Sort By:
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|June 1, 1974
Deficiency of lactosyl sulfatide sulfatase in metachromatic leucodystrophy (sulfatidosis)K Harzer, H U Benz
Journal of Neurochemistry|January 1, 1987
Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophiesK Harzer, B Kustermann-Kuhn
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|November 1, 1973
[Quantitative metachromasia with pseudoisocyanin: a new method for the determination of sulphatides, and for use in the diagnosis of metachromatic leucodystrophy (sulphatide lipidosis) (author's transl)]K Harzer, H U Benz
Humangenetik|October 7, 1975
Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophyK Harzer, A S Recke
Human Genetics|January 1, 1983
Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymogramsB Kustermann-Kuhn, K Harzer
Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1981
[Problems in the diagnosis of metachromatic leukodystrophy by arylsulfatase-A assay in white blood cells. Genetic study of normal enzyme values in 64 mother and child pairs (author's transl)]K Harzer, K I Gussmann
Acta Neuropathologica|February 28, 1974
Metachromatic reaction of pseudoisocyanine with sulfatides in metachromatic leukodystrophy (MLD). I. Technique of histochemical stainingH U Benz, K Harzer
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 16, 2001
Quantified increases of cholesterol, total lipid and globotriaosylceramide in filipin-positive Niemann-Pick type C fibroblastsK Harzer, B Kustermann-Kuhn
Neuropediatrics|May 1, 1984
Diffuse-disseminated sclerosis combined with partial arylsulfatase A (ASA) deficiency. Mixed heterozygosity of ASA- and pseudo-ASA-deficiency?J Peiffer, K Harzer, W Schlote
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1981
[Infantile and late-onset type of globoid cell leucodystrophy in one family (author's transl)]H Böhles, R Schlenk, K Harzer
Pageof 13

Showing results (31-40 of 126) with videos related to

Sort By:
Pageof 13
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie|June 1, 1974
Deficiency of lactosyl sulfatide sulfatase in metachromatic leucodystrophy (sulfatidosis)K Harzer, H U Benz
Journal of Neurochemistry|January 1, 1987
Brain galactolipid content in a patient with pseudoarylsulfatase A deficiency and coincidental diffuse disseminated sclerosis, and in patients with metachromatic, adreno-, and other leukodystrophiesK Harzer, B Kustermann-Kuhn
Zeitschrift Fur Klinische Chemie Und Klinische Biochemie|November 1, 1973
[Quantitative metachromasia with pseudoisocyanin: a new method for the determination of sulphatides, and for use in the diagnosis of metachromatic leucodystrophy (sulphatide lipidosis) (author's transl)]K Harzer, H U Benz
Humangenetik|October 7, 1975
Sulfatide excreting heterozygous carrier of juvenile metachromatic leukodystrophy or asymptomatic patient of adult metachromatic leukodystrophyK Harzer, A S Recke
Human Genetics|January 1, 1983
Prenatal diagnosis of Tay-Sachs disease. Reflectometry of hexosaminidase A, B, and C/S bands on zymogramsB Kustermann-Kuhn, K Harzer
Archiv Fur Psychiatrie Und Nervenkrankheiten|January 1, 1981
[Problems in the diagnosis of metachromatic leukodystrophy by arylsulfatase-A assay in white blood cells. Genetic study of normal enzyme values in 64 mother and child pairs (author's transl)]K Harzer, K I Gussmann
Acta Neuropathologica|February 28, 1974
Metachromatic reaction of pseudoisocyanine with sulfatides in metachromatic leukodystrophy (MLD). I. Technique of histochemical stainingH U Benz, K Harzer
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 16, 2001
Quantified increases of cholesterol, total lipid and globotriaosylceramide in filipin-positive Niemann-Pick type C fibroblastsK Harzer, B Kustermann-Kuhn
Neuropediatrics|May 1, 1984
Diffuse-disseminated sclerosis combined with partial arylsulfatase A (ASA) deficiency. Mixed heterozygosity of ASA- and pseudo-ASA-deficiency?J Peiffer, K Harzer, W Schlote
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1981
[Infantile and late-onset type of globoid cell leucodystrophy in one family (author's transl)]H Böhles, R Schlenk, K Harzer
Pageof 13