CĂRȚI ÎN ENGLEZĂ ÎN LEGĂTURĂ CU «FANCONI ANAEMIA»
Descoperă întrebuințarea
Fanconi anaemia în următoarea selecție bibliografică. Cărți în legătură cu
Fanconi anaemia și extrase din aceasta pentru a furniza contextul de întrebuințare al acestuia în literatura Engleză.
1
Fanconi Anemia: A Paradigmatic Disease for the Understanding ...
6 Strathdee CA, Gavish H, Shannon WR, Buchwald M: Cloning of cDNAs for
Fanconi's anaemia by functional complementation. Nature 1992;356:763–767. 7
de Winter JP, Leveille F, van Berkel CG, Rooimans MA, van Der Weel L, et al: ...
... Schindler-Hoehn, Holger Hoehn, 2007
2
Blood: Principles and Practice of Hematology
Hepatic rumours during androgen 356. therapy in Fanconi anaemia. Eur J
Pediatr 1993;152:691-693. 320. Sanchez MD, Cantoni AC, Alvarez BM, et al.
Clinical and cytogenetic van- 357. ability on twelve Fanconi anemia and its
relationship ...
Robert I. Handin, Samuel E. Lux, Thomas P. Stossel, 2003
3
Genetic Predisposition to Cancer, 2Ed
Strathdee CA, Duncan AM, Buchwald M. Evidence for at least four Fanconi
anaemia genes including FACC on chromosome 9. Nature Genet 1992; 1:196–
198. Joenje H, Oostra AB, Wijker M, et al. Evidence for at least eight Fanconi
anemia ...
Ros Eng, Douglas Easton, Bruce Ponder, 2004
4
Recent Advances in Haematology
Fanconi's anaemia is diagnosed by demonstrating increased breaks, gaps,
rearrangements, exchange and reduplication in metaphase preparation of
cultured peripheral blood lymphocytes. Breakage of chromosomes dramatically
increases ...
5
Clinically Relevant Resistance in Cancer Chemotherapy
Strathdee CA, Gavish H, Shannon WR, Buchwald M. Cloning of cDNAs for
Fanconi's anaemia by functional complementation. Nature, 358:434-436, 1992.
99. Lo Ten Foe JR, Rooimans MA, Bosnoyan-Collins L, et al Expression cloning
of a ...
Borje Andersson, David Murray, David Murray (Ph.D.), 2002
6
Thomas' Hematopoietic Cell Transplantation
Strathdee CA, Gavish H, Shannon WR, Buchwald M. Cloning of cDNAs for
Fanconi's anaemia by functional complementation. Nature 1992; 358:763–7. 41
a Lo Ten Foe JR, Rooimans MA, Bosnoyan-Collins L et al. Expression cloning of
a ...
Frederick R. Appelbaum, Stephen J. Forman, Robert S. Negrin, 2011
7
Nursing in Haematological Oncology
Birth Defects 18:167–174 Davis S M, Khan S, Wagner J E et al 1996 Unrelated
bone marrow transplantation for Fanconi's anaemia. Bone Marrow
Transplantation 17:43–47 Dokal I 1996a Severe aplastic anaemia including
Fanconi's anaemia ...
Alter BP, Frissora CL, Halperin DS et al. Fanconi's anaemia and pregnancy.
BrJHaematol 1991; 77: 410–18. Gluckman E, Devergie A, Schaison G et al. Bone
marrow transplantation in Fanconi anaemia. Br J Haematol 1980; 45: 557–64.
Robert J. Arceci, Ian M. Hann, Owen P. Smith, 2008
9
Congenital Disorders of Erythropoiesis
Blood 10, 788-801 CROSSEN, P.E., MELLOR, J.E.L., ADAMS, A.C. & GUNZ, F.W.
(1972) Chromosome studies in Fanconi's anaemia before and after treatment
with oxymetholone. Pathology 4, 27-33 DACIE, J.V. & GILPIN, A. (1944)
Refractory ...
CIBA Foundation Symposium, 2009
10
Postgraduate Haematology
All inherited bone marrow failure syndromes Alter BP, Young NS (1998) The
bone marrow failure syndromes. In: Haematology of Infancy and Childhood (DG
Nathan, HS Orkin, eds), pp. 237–335. WB Saunders, Philadelphia. Fanconi
anaemia ...
A. Victor Hoffbrand, Daniel Catovsky, Edward G. D. Tuddenham, 2011
ȘTIRI NOI CARE INCLUD TERMENUL «FANCONI ANAEMIA»
Află ce ziare naționale și internaționale au scris despre și cum este întrebuințat termenul
Fanconi anaemia în contextul următoarelor știri.
Family of Eastbourne 11-year-old awaiting a bone marrow …
Dylan is awaiting a bone marrow transplant for a rare genetic condition called Fanconi Anaemia. A donor has been found and he will undergo ... «Eastbourne Herald, Iun 15»
Lakshan is off to India – thanks to the overwhelming response
The boy is suffering from Fanconi anaemia, a rare inherited blood disorder, for which the only answer is a bone marrow transplant. The family ... «The Sunday Times Sri Lanka, Iun 15»
Cancer kids are thankful to Megan
The money raised is being donated to the Anthony Nolan Trust as two of Megan's friends, James and Emma, suffer from Fanconi Anaemia, and ... «Linlithgow Journal & Gazette, Iun 15»
Cure close at hand
... Beckwith-Wiedemann syndrome, Fanconi anaemia syndrome, Noonan syndrome and Von Hippel-Lindau syndrome also increase the risk of ... «Deccan Herald, Mai 15»
Exclusive Interview: 12-year-old undergoes successful first 'half …
A rare genetic disorder, Fanconi anaemia is a type of inherited bone marrow failure syndrome. In this, the patient's body is unable to produce ... «TheHealthSite, Mai 15»
Iraqi child undergoes rare surgery in Gurgaon
Fanconi Anaemia is a rare disease - a kind of inherited bone marrow failure syndrome where the body of the patient does not make red blood ... «Zee News, Mai 15»
Malaysian wins Oxford prize
“In Fanconi anaemia, for example, the mutation in that protein causes developmental defect and higher occurrences of cancer, and makes the ... «New Straits Times Online, Apr 15»
County Durham boy's life saved thanks to international donor
Alfie, of Consett, is believed to have suffered from a little known condition called Fanconi anaemia (FA), a rare genetic disease, since birth. «ChronicleLive, Mar 15»
Natural health with Megan Sheppard: Scabies and Pancytopenia
... leukaemia, aplastic anaemia, myelofibrosis, malignant osteoporosis, and Fanconi anaemia. It can also be a side effect of certain medications. «Irish Examiner, Mar 15»
Francesca turns scientist to learn about her blood
Francesca Evans-Jones, from Lancing, was diagnosed with Fanconi Anaemia in April 2014. Since then, Francesca has made numerous visits ... «Worthing Herald, Mar 15»
