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Showing 1 to 12 of 280 entries
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Successful treatment of a Caucasian case of multifocal Castleman's disease with TAFRO syndrome with a pathophysiology targeted therapy - a case report.

Experimental hematology & oncology

Tedesco S, Postacchini L, Manfredi L, Goteri G, Luchetti MM, Festa A, Gabrielli A, Pomponio G.
PMID: 25671135
Exp Hematol Oncol. 2015 Jan 14;4(1):3. doi: 10.1186/2162-3619-4-3. eCollection 2015.

BACKGROUND: Castleman-Kojima disease (TAFRO Syndrome) is characterized by Thrombocytopenia, Anasarca, myeloFibrosis, Renal dysfunction, Organomegaly, multiple lymphadenopathy and histopathology pattern of atypical Castleman's disease (CD). Only few cases of this recently identified unique variant of Multicentric CD (MCD) are described...

Editorial Introduction.

Journal of genetic counseling

Resta RG.
PMID: 26140906
J Genet Couns. 1997 Dec;6(4):373-4. doi: 10.1023/A:1025640625004.

No abstract available.

Genetic Library.

Journal of genetic counseling

Resta RG.
PMID: 26142110
J Genet Couns. 1999 Jun;8(3):183-6. doi: 10.1023/A:1022838807403.

No abstract available.

Genetic Library.

Journal of genetic counseling

Resta RG.
PMID: 26141321
J Genet Couns. 2000 Jun;9(3):267-70. doi: 10.1023/A:1009420122804.

No abstract available.

Cord Blood as a Source of Natural Killer Cells.

Frontiers in medicine

Mehta RS, Shpall EJ, Rezvani K.
PMID: 26779484
Front Med (Lausanne). 2016 Jan 05;2:93. doi: 10.3389/fmed.2015.00093. eCollection 2015.

Cord blood (CB) offers several unique advantages as a graft source for hematopoietic stem cell transplantation (HSCT). The risk of relapse and graft vs. host disease after cord blood transplantation (CBT) is lower than what is typically observed after...

Engineering cord blood to improve engraftment after cord blood transplant.

Stem cell investigation

Mehta RS, Dave H, Bollard CM, Shpall EJ.
PMID: 28607915
Stem Cell Investig. 2017 May 25;4:41. doi: 10.21037/sci.2017.05.01. eCollection 2017.

Umbilical cord blood transplant (CBT) has traditionally been associated with slower engraftment of neutrophils, delayed immune reconstitution and consequently higher risk of infections as compared with peripheral blood progenitor cell (PBPC) or bone marrow (BM) transplants. This is primarily...

Genetic library.

Journal of genetic counseling

Resta RG.
PMID: 24242231
J Genet Couns. 1993 Mar;2(1):63-5. doi: 10.1007/BF00962559.

No abstract available.

Genetic library.

Journal of genetic counseling

Resta RG.
PMID: 24242319
J Genet Couns. 1993 Jun;2(2):115-7. doi: 10.1007/BF00962543.

No abstract available.

The crane's foot: The rise of the pedigree in human genetics.

Journal of genetic counseling

Resta RG.
PMID: 24242747
J Genet Couns. 1993 Dec;2(4):235-60. doi: 10.1007/BF00961574.

The standard pedigree used by geneticists is intimately connected to the history of genetics. Pedigrees drawn today are based on standards established in the early decades of the twentieth century. Those standards were established by geneticists who pursued an...

Editorial introduction.

Journal of genetic counseling

Resta RG.
PMID: 24234721
J Genet Couns. 1996 Dec;5(4):153-4. doi: 10.1007/BF01408369.

No abstract available.

Background Parenchymal Enhancement of the Contralateral Normal Breast: Association with Tumor Response in Breast Cancer Patients Receiving Neoadjuvant Chemotherapy.

Translational oncology

Chen JH, Yu HJ, Hsu C, Mehta RS, Carpenter PM, Su MY.
PMID: 26055178
Transl Oncol. 2015 Jun;8(3):204-9. doi: 10.1016/j.tranon.2015.04.001.

PURPOSE: This study investigated the association between background parenchymal enhancement (BPE) and pathologic response to neoadjuvant chemotherapy (NAC).METHODS: A total of 46 patients diagnosed with invasive breast cancer were analyzed. Each patient had three magnetic resonance imaging (MRI) studies,...

Minimal change disease: a variant of lupus nephritis.

NDT plus

Moysés-Neto M, Costa RS, Rodrigues FF, Vieira Neto OM, Reis MA, Louzada Júnior P, Romão EA, Dantas M.
PMID: 25984093
NDT Plus. 2011 Feb;4(1):20-2. doi: 10.1093/ndtplus/sfq179. Epub 2010 Oct 22.

Some patients with systemic lupus erythematosus (SLE) present with nephrotic syndrome due to minimal change disease (MCD). Histopathological diagnosis of patients with SLE and nephrotic-range proteinuria has shown that these patients present with diffuse proliferative glomerulonephritis and membranous glomerulonephritis,...

Showing 1 to 12 of 280 entries