Zobrazeno 1 - 10
of 281
pro vyhledávání: '"William Krivit"'
Publikováno v:
Cell Transplantation, Vol 4 (1995)
Treatment and potential cure of lysosomal and peroxisomal diseases, heretofore considered fatal, has become a reality during the past decade. Bone marrow transplantation, (BMT), has provided a method for replacement of the disease-causing enzyme defi
Externí odkaz:
https://doaj.org/article/5f66ae6f54704237801eecc377605b59
Autor:
William Krivit, Sven Hammarström
Publikováno v:
Journal of Lipid Research, Vol 13, Iss 4, Pp 525-530 (1972)
Free ceramides were isolated from human platelets. Their structures were unequivocally determined by gas–liquid chromatography–mass spectrometry of the trimethylsilyl ether derivatives. The major components were N-(palmitoyl) sphingosine, N-(stea
Externí odkaz:
https://doaj.org/article/fc00339663b04727953502374c92cdf9
Publikováno v:
Journal of Lipid Research, Vol 13, Iss 1, Pp 128-136 (1972)
Analyses have been made of glycosphingolipids from visceral organs and brain of a patient with an unusual lipid storage disorder diagnosed initially as classical Tay-Sachs disease. Levels of the lipids from fresh-frozen sections of gray and white mat
Externí odkaz:
https://doaj.org/article/d8946c397e2c42978c0a06997eb6ac5d
Publikováno v:
Journal of Lipid Research, Vol 10, Iss 2, Pp 188-192 (1969)
Concentrations of four neutral glycosyl ceramides were determined in plasma and erythrocytes from nine hemizygous patients with Fabry's disease (a hereditary glycolipid lipidosis), from the sister of one of the patients, and from the heterozygous mot
Externí odkaz:
https://doaj.org/article/4e2df5eab7b648f2ad38ac4668a0bdb3
Publikováno v:
Journal of Developmental & Behavioral Pediatrics. 27:290-296
Advances in medical treatment have prolonged the lives of children with Hurler syndrome or mucopolysaccharidosis I requiring increased attention to the assessment of their long-term outcomes and functional abilities. Adaptive functions are critical f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ac5b76b3e1bcf433d5a7a21e3b2afd0
https://doi.org/10.1097/00004703-200608000-00002
https://doi.org/10.1097/00004703-200608000-00002
Autor:
William Krivit
Publikováno v:
Springer Seminars in Immunopathology. 26:119-132
This is a review of the clinical responses and prospectus of new therapies following use of allogeneic hematopoietic stem cell transplantation for the treatment of the following disorders: Hurlers syndrome (MPS 1-H), globoid cell leukodystrophy (GLD;
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45280267e12277cfbf6e846471138a46
https://doi.org/10.1007/s00281-004-0166-2
https://doi.org/10.1007/s00281-004-0166-2
Autor:
Paul J. Orchard, Elsa Shapiro, Frank L. Rimell, Satkiran S. Grewal, Charles Peters, Stella M. Davies, John E. Wagner, Kathleen A. Delaney, S Abel, Lawrence R. Charnas, William Krivit, Alfred C. Grovas, David A. Wenger, Lawrence A. Lockman
Publikováno v:
The Journal of Pediatrics. 144:569-573
Objectives To study the efficacy of hematopoietic stem cell transplantation (HCT) for ameliorating the clinical manifestations of α-mannosidosis. Study design Four patients with α-mannosidosis underwent allogeneic HCT at the University of Minnesota
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49bc8b97f94a5db3917a4f094a6a5646
https://doi.org/10.1016/j.jpeds.2004.01.025
https://doi.org/10.1016/j.jpeds.2004.01.025
Autor:
Carol J. Holman, J. E. Julin, J. H. Van Burik, H. B. Clark, William Krivit, Chiu Ho Webb, Henry H. Balfour
Publikováno v:
Transplant Infectious Disease. 4:201-206
A 20-year-old patient, who received a bone marrow transplant in order to treat metachromatic leukodystrophy (MLD), succumbed to cytomegalovirus (CMV) encephalitis. After CMV viremia developed, the patient received ganciclovir, but he was switched to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b29cde025cae23838fa617f7a057351
https://doi.org/10.1034/j.1399-3062.2002.02005.x
https://doi.org/10.1034/j.1399-3062.2002.02005.x
Autor:
Xavier Montalban, N. Raguer, William Krivit, John S. Waye, Barry Eng, C. Borràs, Carmen Domínguez, Carmen Navarro, Manuel Comabella
Publikováno v:
Annals of Neurology. 50:108-112
We report the case of a 50-year-old woman and her 32-year-old daughter, both of whom are affected with adult-onset metachromatic leukodystrophy (MLD) clinically presenting as peripheral neuropathy. Arylsulfatase A (ARSA) activities were markedly redu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::00b76bf9e3b81b26b834fbf5b32cde19
https://doi.org/10.1002/ana.1076
https://doi.org/10.1002/ana.1076
Publikováno v:
Current Opinion in Neurology. 12:167-176
Over 400 patients with lysosomal and peroxisomal storage diseases have received hematopoietic stem cell transplantation from normal donors. Without treatment, all of these diseases have an inexorable fate leading to central nervous system deteriorati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd541288b90276eaa18735265a4a5f5b
https://doi.org/10.1097/00019052-199904000-00007
https://doi.org/10.1097/00019052-199904000-00007