Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Linda, Cabral"'
Publikováno v:
Rhode Island medical journal (2013). 104(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::77a4d3d6008c689a7371b2cdefda147a
https://pubmed.ncbi.nlm.nih.gov/33926150
https://pubmed.ncbi.nlm.nih.gov/33926150
Autor:
Sloane Cammock, Linda Cabral, Anant Vatsayan, Rachel A. Egler, Shahrazad Saab, Ravi Talati, Jignesh Dalal, Amy Dimarino, Kristen Nagle
Publikováno v:
Journal of Pediatric Hematology/Oncology. 40:e315-e318
Lymphoid interstitial pneumonia (LIP) is a rare disease characterized by benign reactive polyclonal proliferation of bronchus-associated lymphoid tissue after exposure to inhaled or circulating antigen(s), leading to a disease symptomatology similar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::07878e6de3d1e50ff2d37d2b33159d94
https://doi.org/10.1097/mph.0000000000000977
https://doi.org/10.1097/mph.0000000000000977
Publikováno v:
Rhode Island medical journal (2013). 102(5)
As the Patient Centered Medical Home (PCMH) model has evolved nationally and in Rhode Island, there has been increased recognition that PCMH has not been sufficient to achieve desired cost and quality goals. In this article, we describe the evolving
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::362b443211132f971351a0fc2e039046
https://pubmed.ncbi.nlm.nih.gov/31167524
https://pubmed.ncbi.nlm.nih.gov/31167524
Publikováno v:
Hematology/oncology and stem cell therapy. 12(2)
Hematopoietic stem cell transplant (HSCT) with matched sibling donor (MSD) is considered the first line of therapy for patients with severe aplastic anemia (SAA) who are
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0aacfeb1e32504051261a4c319bd0d1
https://pubmed.ncbi.nlm.nih.gov/30176244
https://pubmed.ncbi.nlm.nih.gov/30176244
Autor:
Hasan Hashem, Linda Cabral, Ghada Abusin, Kenneth R. Cooke, Rupesh Raina, Jeffery J. Auletta, Rolla Abu-Arja, Beth A. Vogt, Prashant Vijayaraghavan
Publikováno v:
Pediatric transplantation. 22(2)
Maintaining fluid balance, pre- and post-MA-HCT is essential and usually requires frequent administration of diuretics. Hepatic sinusoidal obstructive syndrome is potentially life-threatening, especially when associated with AKI and MOF. This study d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4d9644e7927f158c3fd1757db80a72
https://pubmed.ncbi.nlm.nih.gov/29388370
https://pubmed.ncbi.nlm.nih.gov/29388370
Autor:
Kenneth R. Cooke, J. Arnold, Blanca E. Gonzalez, Jeffery J. Auletta, Michael R. Jacobs, Rachel A. Egler, Rolla Abu-Arja, Linda Cabral
Publikováno v:
Transplant Infectious Disease. 16:830-837
We describe the first case, to our knowledge, of disseminated Mycobacterium bovis Bacillus Calmette-Guérin infection in a child with Bare Lymphocyte Syndrome type II after undergoing hematopoietic stem cell transplantation (HSCT). The patient presen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6fc2d3ac7e0000049e8e96a150748e
https://doi.org/10.1111/tid.12263
https://doi.org/10.1111/tid.12263
Autor:
Rachel A. Egler, Leah Chernin, Kenneth R. Cooke, Hans D. Ochs, Haig Tcheurekdjian, Ghada Abusin, Troy R. Torgerson, Rolla Abu-Arja, Jesus M. Lopez-Guisa, Jeffery J. Auletta, Linda Cabral, Robert Hostoffer
Publikováno v:
Pediatric Blood & Cancer. 62:1674-1676
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency characterized by marked reduction in all classes of serum immunoglobulins and the near absence of mature CD19(+) B-cells. Although malignancy has been observed in patients with XLA, we p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11736e08b8b5f26fb305c3a08eba3c84
https://doi.org/10.1002/pbc.25554
https://doi.org/10.1002/pbc.25554
Publikováno v:
Pediatric Transplantation. 22:e13174
HLH occurring after HSCT is a relatively rare disease. Many conditions may mimic or trigger HLH in post-HSCT period (eg, cytokine release syndrome, engraftment syndrome, graft rejection/failure, acute graft-vs-host disease, infections systemic inflam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b6a92d7bec2b6acbec4569b9d830466
https://doi.org/10.1111/petr.13174
https://doi.org/10.1111/petr.13174
Autor:
Linda, Cabral, Christine, Johnson
Publikováno v:
Physician leadership journal. 2(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c8d16d0b7bc02aa2d5f228b0be96e29
https://pubmed.ncbi.nlm.nih.gov/26529881
https://pubmed.ncbi.nlm.nih.gov/26529881
Autor:
Rolla F, Abu-Arja, Leah R, Chernin, Ghada, Abusin, Jeffery, Auletta, Linda, Cabral, Rachel, Egler, Hans D, Ochs, Troy R, Torgerson, Jesus, Lopez-Guisa, Robert W, Hostoffer, Haig, Tcheurekdjian, Kenneth R, Cooke
Publikováno v:
Pediatric bloodcancer. 62(9)
X-linked agammaglobulinemia (XLA) is a primary immunodeficiency characterized by marked reduction in all classes of serum immunoglobulins and the near absence of mature CD19(+) B-cells. Although malignancy has been observed in patients with XLA, we p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::58a2219396c5c1743928e32a8bc118d7
https://pubmed.ncbi.nlm.nih.gov/25900577
https://pubmed.ncbi.nlm.nih.gov/25900577