Cargando…

P-012: FREQUENCY OF INDICATIONS OF HEMATOPOIETIC STEM CELL TRANSPLANT ACCORDING TO DIFFERENT SETS OF INDICATIONS AND ANALYSIS OF COMORBIDITY INDEX SCORES IN BRAZILIAN ADULTS WITH SICKLE CELL DISEASE

Detalles Bibliográficos
Autores principales:	G., SANTOS, K., TOZATTO-MAIO, L., ALVES, G., FONSECA, G., MELO, L., SUGANUMA-OTSUKA, F., NOGUEIRA, A., CARDOSO, S., GUALANDRO, V., ROCHA
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Lippincott Williams & Wilkins 2022
Materias:	Poster Presentations
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9426847/ http://dx.doi.org/10.1097/01.HS9.0000872948.75372.ca

Ejemplares similares

P1494: INDICATIONS OF HEMATOPOIETIC STEM CELL TRANSPLANT ACCORDING TO DIFFERENT SETS OF INDICATIONS AND ANALYSIS OF COMORBIDITY INDEX SCORES IN BRAZILIAN PATIENTS WITH SICKLE CELL DISEASE
por: Santos, G., et al.
Publicado: (2022)

Comorbidity of Glucose-6-Phosphate Dehydrogenase Deficiency and Sickle Cell Disease Exert Significant Effect on RBC Indices
por: Antwi-Baffour, Samuel, et al.
Publicado: (2019)

Extreme hyperbilirubinemia: An indicator of morbidity and mortality in sickle cell disease
por: Haydek, John Paul, et al.
Publicado: (2019)

Hematological Indices of Sickle Cell Anaemia Patients with Pulmonary Tuberculosis in Northern Nigeria.
por: Ahmed, Sagir G., et al.
Publicado: (2010)

The hematopoietic saga of clonality in sickle cell disease
por: Stonestrom, Aaron J., et al.
Publicado: (2022)

Haematological indices of sickle cell patients with chronic leg ulcers on compression therapy
por: Babalola, Oluwatoyin A., et al.
Publicado: (2020)

Differences between reference intervals of blood counts of Brazilian adults with and without sickle cell trait according to laboratory tests from the National Health Survey
por: de Sá, Ana Carolina Micheletti Gomide Nogueira, et al.
Publicado: (2023)

Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease
por: Tozatto-Maio, Karina, et al.
Publicado: (2020)

Brazilian Guidelines for transcranial doppler in children and adolescents with sickle cell disease
por: Lobo, Clarisse Lopes de Castro, et al.
Publicado: (2011)

Hematopoietic Cell Transplantation for Sickle Cell Disease
por: Krishnamurti, Lakshmanan
Publicado: (2021)

Comparative study of 0.2% and 0.12% digluconate chlorhexidine mouth rinses on the level of dental staining and gingival indices
por: Najafi, Mohammad Hassan, et al.
Publicado: (2012)

Blood Transfusion Frequency and Indications in Yemeni Children with Sickle Cell Disease
por: Al-Saqladi, Abdul-Wahab M., et al.
Publicado: (2020)

PW01-012 – Canakinumab in patients with FMF
por: Ugurlu, S, et al.
Publicado: (2013)

Allogeneic Hematopoietic Stem Cell Transplantation for Adults with Sickle Cell Disease
por: Saraf, Santosh L., et al.
Publicado: (2019)

Risk Factors of Pulmonary Hypertension in Brazilian Patients with Sickle Cell Anemia
por: Lobo, Clarisse Lopes de Castro, et al.
Publicado: (2015)

P01-012 – Evaluation of autonomic function in FMF
por: Ayaz, N Aktay, et al.
Publicado: (2013)

Assessment of Some Indicators of Oxidative Stress in Nigerian Sickle Cell Anemic Patients
por: Okorie, C. P., et al.
Publicado: (2018)

Predictivity of the comorbidity indices for geriatric syndromes
por: Canaslan, Kubra, et al.
Publicado: (2022)

Comorbidities in sickle cell disease: Adult providers needed!
por: Ogu, Ugochi O., et al.
Publicado: (2018)

Pulmonary function indices in children with sickle cell anemia in Enugu, south-east Nigeria
por: Achigbu, Kingsley I., et al.
Publicado: (2015)

Erythrocyte indices in Pre-school Nigerian Children with Sickle Cell Anaemia in Steady State
por: Akodu, Samuel Olufemi, et al.
Publicado: (2015)

Hemoglobinopathy is Associated With Total Hip Arthroplasty Indication Even Beyond Sickle Cell Anemia
por: Rakutt, Maxwell J., et al.
Publicado: (2022)

Indication to dynamic and invasive testing in Cushing’s disease according to different neuroradiological findings
por: Ferrante, E., et al.
Publicado: (2021)

The ATLAS Level-1 Central Trigger System 012
por: Borrego-Amaral, P, et al.
Publicado: (2004)

Early Life Inflammation and the Developing Hematopoietic and Immune Systems: The Cochlea as a Sensitive Indicator of Disruption
por: Otsuka, Kelly S., et al.
Publicado: (2021)

Assessment of Panoramic Radiomorphometric Indices of the Mandible in a Brazilian Population
por: Alonso, Maria Beatriz C. C., et al.
Publicado: (2011)

PW03-012 – Unmet need in Behçet's disease: remission is rare
por: Alibaz-Oner, F, et al.
Publicado: (2013)

Mobilizing hematopoietic progenitor cells in donors with sickle cell trait is safe
por: De Santis, Gil Cunha, et al.
Publicado: (2019)

Economic burden of sickle cell disease in Brazil
por: Silva-Pinto, Ana Cristina, et al.
Publicado: (2022)

Characterization of HIV risks in a Brazilian sickle cell disease population
por: Blatyta, P. F., et al.
Publicado: (2020)

Comparative Evaluation of Adiposity Indices as Predictors of Hypertension among Brazilian Adults
por: Dutra, Maurílio T., et al.
Publicado: (2018)

The triglyceride-glucose index as an indicator of insulin resistance and cardiometabolic risk in Brazilian adolescents
por: Reckziegel, Miriam Beatrís, et al.
Publicado: (2023)

Comorbidity indices for clinical trials: adaptation of two existing indices for use with the FREEDOM trial in women with postmenopausal osteoporosis
por: Silverman, S. L., et al.
Publicado: (2015)

Alterations in fetal thymic and liver hematopoietic cells as indicators of exposure to developmental immunotoxicants.
por: Holladay, S D, et al.
Publicado: (1996)

Functional evaluation indicates physical losses after hematopoietic stem cell transplantation
por: de Souza, Clarissa Vasconcellos, et al.
Publicado: (2012)

New Indications for Hematopoietic Stem Cell Gene Therapy in Lysosomal Storage Disorders
por: Rossini, Linda, et al.
Publicado: (2022)

AB012. Brachytherapy for localized prostate cancer
por: Xu, Yong, et al.
Publicado: (2016)

AB012. Update on treatments for premature ejaculation
por: Hyun, Jae-Seog
Publicado: (2017)

Mast Cell Activation Syndrome as a Significant Comorbidity in Sickle Cell Disease
por: Afrin, Lawrence B.
Publicado: (2014)

Hematopoietic Stem Cell Function in a Murine Model of Sickle Cell Disease
por: Javazon, Elisabeth H., et al.
Publicado: (2012)

Cannot write session to /tmp/vufind_sessions/sess_vpit6i0f02es83qcgmnp3dmg8d