W Baier|K Harzer - JoVE Visualize

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American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|July 1, 1994

Controlled trial of backrest elevation after coronary angiographyC Coyne, W Baier, B Perra, et al.

Human Genetics|September 1, 1993

Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage diseaseV Bradová, F Smíd, B Ulrich-Bott, et al.

Oncogene|October 20, 2001

The role of ceramide in receptor- and stress-induced apoptosis studied in acidic ceramidase-deficient Farber disease cellsC Burek, J Roth, H G Koch, et al.

Molecular Genetics and Metabolism|August 5, 2000

Deficient ferritin immunoreactivity in tissues from niemann-pick type C patients: extension of findings to fetal tissues, H and L ferritin isoforms, but also one case of the rare Niemann-Pick C2 complementation groupH Christomanou, M T Vanier, P Santambrogio, et al.

Annual Review of Nutrition|August 15, 2000

Oligosaccharides in human milk: structural, functional, and metabolic aspectsC Kunz, S Rudloff, W Baier, et al.

Pediatric Nephrology (Berlin, Germany)|September 1, 1992

Association of Kawasaki disease and interstitial nephritisP A Veiga, D Pieroni, W Baier, et al.

Biological Chemistry Hoppe-Seyler|January 1, 1994

Further evidence that human lysosomal sialidase is not derived from prosaposin. Prosaposin biosynthesis and ganglioside sialidase studies in prosaposin- and sialidase-deficient fibroblast linesB C Paton, H R Schneider-Jakob, J Kopitz, et al.

Journal of the Neurological Sciences|December 1, 1995

Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsT Levade, H W Moser, A H Fensom, et al.

Neuropediatrics|February 1, 1996

Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies: female adrenoleukodystrophy-like disease and late-onset Krabbe diseaseF Gullotta, J L Hughes, W Wittkowski, et al.

Neuropadiatrie|May 1, 1980

Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase BU Burck, K Harzer, H H Goebel, et al.

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Showing results (71-80 of 133) with videos related to

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Pageof 14

American Journal of Critical Care : an Official Publication, American Association of Critical-Care Nurses|July 1, 1994

Controlled trial of backrest elevation after coronary angiographyC Coyne, W Baier, B Perra, et al.

Human Genetics|September 1, 1993

Prosaposin deficiency: further characterization of the sphingolipid activator protein-deficient sibs. Multiple glycolipid elevations (including lactosylceramidosis), partial enzyme deficiencies and ultrastructure of the skin in this generalized sphingolipid storage diseaseV Bradová, F Smíd, B Ulrich-Bott, et al.

Oncogene|October 20, 2001

The role of ceramide in receptor- and stress-induced apoptosis studied in acidic ceramidase-deficient Farber disease cellsC Burek, J Roth, H G Koch, et al.

Molecular Genetics and Metabolism|August 5, 2000

Deficient ferritin immunoreactivity in tissues from niemann-pick type C patients: extension of findings to fetal tissues, H and L ferritin isoforms, but also one case of the rare Niemann-Pick C2 complementation groupH Christomanou, M T Vanier, P Santambrogio, et al.

Annual Review of Nutrition|August 15, 2000

Oligosaccharides in human milk: structural, functional, and metabolic aspectsC Kunz, S Rudloff, W Baier, et al.

Pediatric Nephrology (Berlin, Germany)|September 1, 1992

Association of Kawasaki disease and interstitial nephritisP A Veiga, D Pieroni, W Baier, et al.

Biological Chemistry Hoppe-Seyler|January 1, 1994

Further evidence that human lysosomal sialidase is not derived from prosaposin. Prosaposin biosynthesis and ganglioside sialidase studies in prosaposin- and sialidase-deficient fibroblast linesB C Paton, H R Schneider-Jakob, J Kopitz, et al.

Journal of the Neurological Sciences|December 1, 1995

Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsT Levade, H W Moser, A H Fensom, et al.

Neuropediatrics|February 1, 1996

Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies: female adrenoleukodystrophy-like disease and late-onset Krabbe diseaseF Gullotta, J L Hughes, W Wittkowski, et al.

Neuropadiatrie|May 1, 1980

Ultrastructural pathology of skin biopsy and fibroblast enzyme studies in a case of GM2-gangliosidosis with deficient hexosaminidase A and thermolabile hexosaminidase BU Burck, K Harzer, H H Goebel, et al.

Pageof 14