نتایج جستجو برای: farber disease

تعداد نتایج: 1490893  

2011
Himshikha Bhutani

Mukherjee dedicates his book to “Robert Sandler” and to all those who fought and continue to fight against cancer. In 1947, two year old Robert was the first leukemic patient to be tested with Farber’s antifolates. Robert even responded to aminopterin, though his cancer relapsed. The journey till the antifolates was not an easy one and it took decades after decades to traverse the path from the...

2014
Anthony Flynn Dawn Van Dam

• Rick Wilson, Director, The Genome Institute at Washington Univ. School of Medicine • Judy Garber, Director, Cancer Risk/Prevention Clinic, Dana Farber • Shashikant Kulkarni, Head of Clinical Genomics, Wash. University School of Medicine • Shyamali Singhal, Medical Director of the Cancer Center, El Camino Hospital • Nickolas Papadopoulos, Director of Translational Genetics, Johns Hopkins Medic...

Journal: :Revista espanola de cardiologia 2009
Nicolás Laffaye Pablo D Comignani

1. Barberá JA, Escribano P, Morales P, Gómez MA, Oribe M, Martínez A, et al. Estándares asistenciales en hipertensión pulmonar. Rev Esp Cardiol. 2008;61:170-84. 2. Angell M. Is academic medicine for sale? N Engl J Med. 2000;342:1516-8. 3. Bodenheimer T. Uneasy alliance —clinical investigators and the pharmaceutical industry. N Engl J Med. 2000;342:1539-44. 4. Campbell EG, Weissman JS, Vogeli C,...

Journal: :Cell stem cell 2010
Achia Urbach Ori Bar-Nur George Q Daley Nissim Benvenisty

Achia Urbach,1,2,4 Ori Bar-Nur,3,4 George Q. Daley,1,2,* and Nissim Benvenisty3,* 1Stem Cell Transplantation Program, Division of Pediatric Hematology/Oncology, Manton Center for Orphan Disease Research, Howard Hughes Medical Institute, Children’s Hospital Boston and Dana Farber Cancer Institute; Division of Hematology, Brigham and Women’s Hospital, Boston, MA 02115, USA 2Department of Biologic...

2016
Jennifer A. Chan Robin Sommers

Management of neuroendocrine tumors (NETs) requires a multidisciplinary approach, as many modalities are useful in this malignancy. Somatostatin receptor analogues (SSAs) are a mainstay of treatment, both for ameliorating symptoms and slowing disease progression, but novel approaches are emerging. At 2015 JADPRO Live, Jennifer A. Chan, MD, MPH, and Robin Sommers, DNP, ANP-BC, AOCNP, both of Dan...

Journal: :Archives of disease in childhood 1965
J M Lauweryns

This study concerns the pathological changes found in the lungs of 55 newborn infants with hyaline membrane disease (HMD). The accepted appearances are a widespread resorption of air with collapse of many alveolar ducts and most alveoli, producing a severe atelectasis. The alveolar ducts and alveoli that remain open are distended and lined by a variable amount of homogeneous acidophilic materia...

2005
Yutaka Hattori Masayuki Shimoda Shinichiro Okamoto Toru Satoh Tsunayuki Kakimoto Yasuo Ikeda

amyloid protein. The aetiology of PH in this patient is still unclear. She was sero-negative for human immunodeficiency virus, and lacked the clinical symptoms that would indicate systemic sclerosis and systemic lupus erythematosus. She did not have preexisting chronic lung and liver disease or congestive heart disease. Direct association of MM with PH is unlikely in this case because dyspnoea ...

2013
Abdulfatah M Alayoubi James C M Wang Bryan C Y Au Stéphane Carpentier Virginie Garcia Shaalee Dworski Samah El-Ghamrasni Kevin N Kirouac Mathilde J Exertier Zi Jian Xiong Gilbert G Privé Calogera M Simonaro Josefina Casas Gemma Fabrias Edward H Schuchman Patricia V Turner Razqallah Hakem Thierry Levade Jeffrey A Medin

Farber disease (FD) is a severe inherited disorder of lipid metabolism characterized by deficient lysosomal acid ceramidase (ACDase) activity, resulting in ceramide accumulation. Ceramide and metabolites have roles in cell apoptosis and proliferation. We introduced a single-nucleotide mutation identified in human FD patients into the murine Asah1 gene to generate the first model of systemic ACD...

2003
Robert J. Henry

L angerhans’ cell histiocytosis (LCH), formerly known as histiocytosis X, is one of a group of poorly understood diseases of histiocytes. The clinical spectrum of disease ranges from the chronic, localized form to an acute leukemia-like disease with a fatal outcome. Alfred Hand was the first to report a case of histiocytosis in 1893.1 Later, in 1941, Farber described this condition when reporti...

Journal: :Journal of Pure and Applied Algebra 2022

The sectional category of a subgroup inclusion H↪G can be defined as the corresponding map between Eilenberg–MacLane spaces. We extend characterization topological complexity aspherical spaces given by Farber, Grant, Lupton and Oprea to context inclusions investigate it means Adamson cohomology theory.

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