Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Guy H. Grayson"'
Publikováno v:
Proc (Bayl Univ Med Cent)
Langerhans cell histiocytosis is a rare hematologic disorder caused by the proliferation of specialized dendritic cells. Pulmonary manifestations occur in 20% to 50% of multisystem disease, but isolated pulmonary disease is rare. Spontaneous pneumoth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7bdb982ea5c31aad5348132067b36a
https://europepmc.org/articles/PMC7787669/
https://europepmc.org/articles/PMC7787669/
Autor:
Elsa Shapiro, Thomas E. Williams, James B. Nachman, John E. Wagner, Pedro A. deAlarcon, Martin R. Klemperer, Clare J. Twist, E. Fred Saunders, Guy H. Grayson, Joanne Kurtzberg, William Krivit, Gregory A. Hale, Charles Peters, P. Jean Henslee-Downey, Morton J. Cowan, James A. Anderson, Carl Lenarsky, Marta K. Rozans, Richard E. Harris
Publikováno v:
Blood. 91:2601-2608
Untreated patients with Hurler syndrome (MPSIH) experience progressive neurologic deterioration and early death. Allogeneic bone marrow transplantation (BMT) ameliorates or halts this course. The Storage Disease Collaborative Study Group was formed t
Publikováno v:
The Journal of Pediatrics. 126:59-61
We describe an infant who had methemoglobinemia related to acidosis, probably on the basis of renal tubular acidosis. Methemoglobinemia may indicate the presence of a clinically significant underlying disorder.
Autor:
Nancy Bunin, Charles Peters, Craig Kollman, William Krivit, Howard J. Weinstein, Janet D. Hegland, Roberta King, Elsa Shapiro, Carl Lenarsky, Morton J. Cowan, James Anderson, John Wagner, Lawrence A. Lockman, Thomas E. Williams, Phyllis Warkentin, Jean E. Sanders, Richard R. Harris, Tom Bowen, Valerie A. Cool, Jean Henslee-Downey, Paige Kaplan, Kathryn Dusenbery, Michael E. Trigg, Leonard Sender, Peter Falk, Seymour Packman, Mary R. Crittenden, Michael Balthazor, Guy H. Grayson
Publikováno v:
Blood. 87(11)
Long-term survival and improved neuropsychological function have occurred in selected children with Hurler syndrome (MPS I H) after successful engraftment with genotypically matched sibling bons marrow transplantation (BMT). However, because few chil