Base de dados : MEDLINE
Pesquisa : C14.907.077 [Categoria DeCS]
Referências encontradas : 2441 [refinar]
Mostrando: 1 .. 10   no formato [Detalhado]

página 1 de 245 ir para página                         

  1 / 2441 MEDLINE  
              next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28234740
[Au] Autor:Com G; Awad S; Trenor CC
[Ad] Endereço:*Department of Pediatric Pulmonary Medicine, University of Southern California, Los Angeles, CA †Department of Pediatrics, Jordan University of Science and Technology, Irbid, Jordan ‡Division of Hematology/Oncology, Vascular Anomalies Center, Boston Children's Hospital §Harvard Medical School, Boston, MA.
[Ti] Título:Delayed Appearance of Cutaneous Lesions of Cutaneovisceral Angiomatosis (CAT) Leading to Misdiagnosis of Immune Thrombocytopenia.
[So] Source:J Pediatr Hematol Oncol;39(4):e236-e239, 2017 May.
[Is] ISSN:1536-3678
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Cutaneovisceral angiomatosis with thrombocytopenia (CAT), also called multifocal lymphangioendotheliomatosis with thrombocytopenia (MLT), is a rare and newly described vascular malformation. Skin manifestations and thrombocytopenia are the hallmark of CAT/MLT, and visceral lesions are described. We report an infant with pulmonary hemorrhage, thrombocytopenia, and antiplatelet antibodies. There was no cutaneous involvement and the child was initially diagnosed with immune thrombocytopenia. Poor response to immune thrombocytopenia-directed therapy raised suspicion for an alternative diagnosis, and the ultimate diagnosis of CAT/MLT was made by lung tissue sampling. Unexpectedly, 2 years after resolution of pulmonary lesions and thrombocytopenia, the child developed typical cutaneous lesions.
[Mh] Termos MeSH primário: Angiomatose/diagnóstico
Púrpura Trombocitopênica Idiopática/diagnóstico
Dermatopatias/patologia
[Mh] Termos MeSH secundário: Angiomatose/patologia
Diagnóstico Diferencial
Erros de Diagnóstico
Progressão da Doença
Seres Humanos
Lactente
Pulmão/patologia
Masculino
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171031
[Lr] Data última revisão:
171031
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170225
[St] Status:MEDLINE
[do] DOI:10.1097/MPH.0000000000000800


  2 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:28087016
[Au] Autor:Wambier CG; Cappel MA; Danilau Ostroski TK; Montemor Netto MR; de Farias Wambier SP; Santos de Jesus BL; Arruda E
[Ad] Endereço:Department of Medicine, State University of Ponta Grossa, Ponta Grossa, Brazil. Electronic address: cwambier@usp.br.
[Ti] Título:Familial outbreak of eruptive pseudoangiomatosis with dermoscopic and histopathologic correlation.
[So] Source:J Am Acad Dermatol;76(2S1):S12-S15, 2017 Feb.
[Is] ISSN:1097-6787
[Cp] País de publicação:United States
[La] Idioma:eng
[Mh] Termos MeSH primário: Angiomatose/patologia
Dermoscopia
Dermatopatias/patologia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Idoso
Exantema/patologia
Feminino
Seres Humanos
Masculino
Meia-Idade
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170115
[St] Status:MEDLINE


  3 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:27819857
[Au] Autor:Malik D; Basher RK; Mittal BR; Jain TK; Bal A; Singh SK
[Ad] Endereço:From the Departments of *Nuclear Medicine, †Histopathology, and ‡Urology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
[Ti] Título:68Ga-PSMA Expression in Pseudoangiomatous Stromal Hyperplasia of the Breast.
[So] Source:Clin Nucl Med;42(1):58-60, 2017 Jan.
[Is] ISSN:1536-0229
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Ga-labeled prostate-specific membrane antigen ligand PET-CT has emerged as a promising technique to evaluate the extent of disease in patients with prostate carcinoma. We are reporting a 63-year-old man with prostatic carcinoma subjected to Ga-prostate-specific membrane antigen ligand PET-CT for initial staging. In addition to the radiotracer uptake in known primary site (prostate), focal increased radiotracer uptake was also noticed in the left breast. Subsequent biopsy of the breast lesion revealed PASH (pseudoangiomatous stromal hyperplasia), which is a benign mesenchymal proliferative lesion that may present clinically as palpable mass requiring further evaluation to rule out malignancy.
[Mh] Termos MeSH primário: Angiomatose/diagnóstico por imagem
Doenças Mamárias/diagnóstico por imagem
Mama/diagnóstico por imagem
Carcinoma/diagnóstico por imagem
Hiperplasia/diagnóstico por imagem
Neoplasias da Próstata/diagnóstico por imagem
[Mh] Termos MeSH secundário: Angiomatose/complicações
Angiomatose/patologia
Biópsia com Agulha de Grande Calibre
Mama/patologia
Doenças Mamárias/complicações
Doenças Mamárias/patologia
Carcinoma/complicações
Seres Humanos
Hiperplasia/complicações
Hiperplasia/patologia
Masculino
Meia-Idade
Compostos Organometálicos
Neoplasias da Próstata/complicações
Compostos Radiofarmacêuticos
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 ((68Ga)Glu-urea-Lys(Ahx)-HBED-CC); 0 (Organometallic Compounds); 0 (Radiopharmaceuticals)
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170112
[Lr] Data última revisão:
170112
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161108
[St] Status:MEDLINE


  4 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27701670
[Au] Autor:Chuh A; Panzer R; Rosenthal AC; Proksch E; Kempf W; Zawar V; Fickenscher H; Fölster-Holst R
[Ad] Endereço:Jockey Club School of Public Health and Primary Care, The Chinese University of Hong Kong and the Prince of Wales Hospital, Shops 5 and 6, The Imperial Terrace, 356 Queen's Road West, G/F, Shatin, Hong Kong. antonio.chuh@yahoo.com.hk.
[Ti] Título:Annular Eruptive Pseudoangiomatosis and Adenovirus Infection: A Novel Clinical Variant of Paraviral Exanthems and a Novel Virus Association.
[So] Source:Acta Derm Venereol;97(3):354-357, 2017 Mar 10.
[Is] ISSN:1651-2057
[Cp] País de publicação:Sweden
[La] Idioma:eng
[Ab] Resumo:Eruptive pseudoangiomatosis is a distinct exanthem thought to be caused by viruses. The usual rash configu-ration is erythematous papules and macules. An association with echovirus infection has been reported. We present here one adult and one child with this exanthem, supported by clinical, histopathological, and immunohistochemical findings. Both patients presented with prodromal symptoms, widespread angioma-like macules in annular configuration, blanchable telangiectasia, followed by spontaneous remission in 6-8 weeks. Lesional histopathology of the adult patient revealed dilated dermal blood vessels and lymphohistiocytic infiltrates predominated by CD4+ lymphocytes with a 5:1 ratio of CD4:CD8 lymphocytes. No B cells or CD56+ natural killer cells were found. Serology of both patients revealed evidence of active infections by adenoviruses, and a range of other viruses were excluded. We believe that these 2 patients manifested annular eruptive pseudoangio-matosis, a novel variant of the rash with a probable adenovirus association that has not yet been reported.
[Mh] Termos MeSH primário: Infecções por Adenoviridae/virologia
Adenoviridae/patogenicidade
Angiomatose/virologia
Exantema/virologia
Pele/virologia
[Mh] Termos MeSH secundário: Adenoviridae/imunologia
Infecções por Adenoviridae/diagnóstico
Infecções por Adenoviridae/imunologia
Angiomatose/diagnóstico
Angiomatose/imunologia
Biópsia
Pré-Escolar
Exantema/diagnóstico
Exantema/imunologia
Seres Humanos
Imuno-Histoquímica
Masculino
Remissão Espontânea
Pele/imunologia
Pele/patologia
Fatores de Tempo
Adulto Jovem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170320
[Lr] Data última revisão:
170320
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161005
[St] Status:MEDLINE
[do] DOI:10.2340/00015555-2541


  5 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27450985
[Au] Autor:Kelten Talu C; Boyaci C; Leblebici C; Hacihasanoglu E; Bozkurt ER
[Ad] Endereço:1 Istanbul Research and Training Hospital, Pathology Department, Fatih, Istanbul, Turkey.
[Ti] Título:Pseudoangiomatous Stromal Hyperplasia in Core Needle Biopsies of Breast Specimens.
[So] Source:Int J Surg Pathol;25(1):26-30, 2017 Feb.
[Is] ISSN:1940-2465
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Pseudoangiomatous stromal hyperplasia (PASH) is a benign lesion of myofibroblasts that is composed of a network of slit-like channels that resemble vascular spaces. The aims of this study were to document the frequency of PASH in core needle biopsy specimens (CNBS) of the breast, to describe which histopathologic findings coexist with PASH and to examine any endothelial cell differentiation. MATERIALS AND METHODS: We reevaluated hematoxylin and eosin-stained sections of all CNBS that were obtained during a 1-year period. First, we performed CD34 and CD31 immunostainings to highlight the areas of PASH, then performed D2-40/podoplanin (lymphatic endothelial marker) and Fli-1 (vascular endothelial cell marker) immunostains. RESULTS: The total number of CNBS was 412. Areas of PASH were noted in 37 of the 412 cases (9%), with a mean age of 38.5 years. The lesions that were described in association with PASH were "benign breast parenchyma with stromal fibrosis" (17/37; 46%), "fibroepithelial tumors" (17/37; 46%), "columnar cell changes (CCC)" (2/37; 5%), and "invasive carcinoma" (1/37; 3%). There were 2 cases of CCC within the foci of PASH (direct contact with PASH), and 8 additional cases of CCC that coexisted in the same specimen but were not in direct contact. There was no staining for D2-40 or Fli-1 within PASH foci. CONCLUSION: PASH lesions occurred with a frequency of 9% in CNBS and were mostly in association with benign breast lesions in premenopausal women. CCC was determined as an accompanying epithelial lesion within or near PASH areas. No obvious immunopositivity compatible with endothelial cell differentiation was revealed.
[Mh] Termos MeSH primário: Angiomatose/patologia
Doenças Mamárias/patologia
Hiperplasia/patologia
[Mh] Termos MeSH secundário: Adolescente
Adulto
Biomarcadores/análise
Biópsia com Agulha de Grande Calibre
Feminino
Seres Humanos
Imuno-Histoquímica
Meia-Idade
Estudos Retrospectivos
Células Estromais/patologia
Adulto Jovem
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Biomarkers)
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170419
[Lr] Data última revisão:
170419
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:160725
[St] Status:MEDLINE
[do] DOI:10.1177/1066896916660763


  6 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:28329566
[Au] Autor:Ho JD; Wolpowitz D; Phillips TJ
[Ad] Endereço:Department of Dermatology, Boston University School of Medicine, Boston, MA Department of Dermatology and Section of Dermatopathology, Boston University School of Medicine, Boston, MA. jdho@bu.edu.
[Ti] Título:Breast nodularity and ulceration: diffuse dermal angiomatosis a corticosteroid responsive disease.
[So] Source:Dermatol Online J;22(11), 2016 Nov 15.
[Is] ISSN:1087-2108
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Diffuse dermal angiomatosis of the breast (DDAB) is an uncommon ulcerative angiomatosis, which occurs in middle aged women with large pendulous breasts, a history of cigarette smoking, and risk factors for atherosclerosis. Based on its rarity, no well-defined therapeutic regimen has been elucidated. We report a case of DDAB in a woman with no history of smoking or radiographic evidence of occluded vasculature who presented with ulceration and pain-associated breast nodularity. She had a complete reproducible response to oral corticosteroids.
[Mh] Termos MeSH primário: Angiomatose/diagnóstico
Doenças Mamárias/diagnóstico
Úlcera Cutânea/diagnóstico
[Mh] Termos MeSH secundário: Angiomatose/tratamento farmacológico
Angiomatose/patologia
Doenças Mamárias/tratamento farmacológico
Doenças Mamárias/patologia
Feminino
Glucocorticoides/uso terapêutico
Seres Humanos
Meia-Idade
Prednisona/uso terapêutico
Dermatopatias/diagnóstico
Dermatopatias/tratamento farmacológico
Dermatopatias/patologia
Úlcera Cutânea/tratamento farmacológico
Úlcera Cutânea/patologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
0 (Glucocorticoids); VB0R961HZT (Prednisone)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171011
[Lr] Data última revisão:
171011
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170323
[St] Status:MEDLINE


  7 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:27870798
[Au] Autor:Ravera V; Bottoni F; Giani A; Cigada M; Staurenghi G
[Ad] Endereço:Eye Clinic, Department of Clinical Science "Luigi Sacco", Luigi Sacco Hospital, University of Milan, Milan, Italy.
[Ti] Título:RETINAL ANGIOMATOUS PROLIFERATION DIAGNOSIS: A Multiimaging Approach.
[So] Source:Retina;36(12):2274-2281, 2016 Dec.
[Is] ISSN:1539-2864
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:PURPOSE: To identify signs occurring more frequently in retinal angiomatous proliferation (RAP) lesions compared with other types of choroidal neovascularization (CNV) in age-related macular degeneration. METHODS: In this cross-sectional retrospective study, 30 patients were evaluated. These signs were correlated with the type of CNV: shunting of blood flow to the lesion by fluorescein angiography, late leakage by indocyanine green angiography, intraretinal cysts and retinal pigmented epithelium interruption along the retinal pigmented epithelium detachment with a hyperreflective oval area by spectral domain optical coherence tomography, and presence of reticular pseudodrusen by infrared light. RESULTS: Shunting of blood flow was found in 56% of RAP, whereas it was absent in 100% of other CNVs. Late leakage in indocyanine green angiography occurred in all RAP cases, while it was found in 7% of other CNVs. Intraretinal cysts were detected in 100% of RAP cases and in 14% of other CNVs. Retinal pigmented epithelium interruption along the retinal pigmented epithelium detachment was evident in 93% of RAP cases and in 15% of other CNVs. Reticular pseudodrusen were present in 87% of RAP cases and in 21% of other CNVs. CONCLUSION: All the signs investigated were strongly associated to RAP lesions. A multimodal imaging approach may help differentiating subtypes of neovascularization.
[Mh] Termos MeSH primário: Angiomatose/diagnóstico por imagem
Neovascularização de Coroide/diagnóstico por imagem
Degeneração Macular/diagnóstico por imagem
Imagem Multimodal
Neovascularização Retiniana/diagnóstico por imagem
[Mh] Termos MeSH secundário: Idoso
Idoso de 80 Anos ou mais
Estudos Transversais
Feminino
Angiofluoresceinografia/métodos
Seres Humanos
Verde de Indocianina
Masculino
Meia-Idade
Descolamento Retiniano/diagnóstico
Epitélio Pigmentado da Retina/patologia
Estudos Retrospectivos
Tomografia de Coerência Óptica/métodos
Acuidade Visual
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
IX6J1063HV (Indocyanine Green)
[Em] Mês de entrada:1706
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161122
[St] Status:MEDLINE


  8 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27847080
[Au] Autor:Tang EK; Chu PT; Goan YG; Hsieh PP; Lin JC
[Ad] Endereço:Division of Thoracic Surgery, Department of Surgery, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan. Electronic address: ektang@mail2000.com.tw.
[Ti] Título:Dumbbell-Mimicked Mediastinal Angiomatosis.
[So] Source:Ann Thorac Surg;102(6):e555-e556, 2016 Dec.
[Is] ISSN:1552-6259
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Angiomatosis is a nonneoplastic proliferative vascular lesion, which occurs mostly in diverse soft tissues. We observed a rare case of mediastinal angiomatosis with intraspinal invasion that mimicked a dumbbell tumor in a 63-year-old man with a history of prostate adenocarcinoma. A roentgenogram of the chest showed that the patient had left pleural effusion and a left paraspinal mass, computed tomography disclosed a low-density fusiform lesion over the left paraspinal region, and magnetic resonance imaging confirmed a large posterior mediastinal tumor with T4 intraspinal invasion. The tumor was completely excised through a laminectomy of the T3-5 spine, followed by thoracoscopic removal of the mediastinal part. The definitive diagnosis was angiomatosis. Surgical removal of such a dumbbell-mimicked tumor is mandatory because it may progress to spinal cord compression.
[Mh] Termos MeSH primário: Angiomatose/diagnóstico por imagem
Neoplasias do Mediastino/diagnóstico por imagem
[Mh] Termos MeSH secundário: Angiomatose/patologia
Diagnóstico Diferencial
Seres Humanos
Imagem por Ressonância Magnética
Masculino
Neoplasias do Mediastino/patologia
Meia-Idade
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1704
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:161117
[St] Status:MEDLINE


  9 / 2441 MEDLINE  
              first record previous record next record last record
seleciona
para imprimir
Fotocópia
[PMID]:27787381
[Au] Autor:Najm A; Soltner-Neel E; Le Goff B; Guillot P; Maugars Y; Berthelot JM
[Ad] Endereço:Rheumatology Department, Pôle Hospitalo-Universitaire 4, Hôpital Hôtel-Dieu, Centre Hospitalo-Universitaire de Nantes, Nantes Cedex 1, France.
[Ti] Título:Cystic angiomatosis, a heterogeneous condition: Four new cases and a literature review.
[So] Source:Medicine (Baltimore);95(43):e5213, 2016 Oct.
[Is] ISSN:1536-5964
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Cystic angiomatosis (CA) is a rare disorder causing bony cysts. It displays some similarity to Gorham-Stout disease (GSD), but has a much better local prognosis, despite the larger number of cysts. These 2 conditions also differ in terms of their location, visceral involvement, and response to treatment. METHODS: We report 4 cases of CA, including 1 sclerosing form, which we compare with cases from a literature review performed with PRISMA methodology. RESULTS: We reviewed 38 articles describing 44 other patients. Mean age at diagnosis for the 48 patients (our 4 patients + the 44 from the review) was 22.5 years, and 28 of the patients were men. The femur was involved in 81% (n = 39), the pelvis in 73% (n = 35), the humerus in 52% (n = 25), the skull in 48% (n = 23), and the vertebrae in 44% (n = 21). Visceral lymphangiomatosis (either clinical, or detected on autopsy) was also reported in 35% (n = 18) of the patients. The spleen was the most frequently involved organ (n = 12), followed by the lungs and pleura (n = 8). Liver cysts and/or chylothorax were rarely reported (5 cases), but were invariably fatal. Radiation therapy on bone or soft tissue masses was ineffective, as was interferon alpha, in the 2 patients in which this drug was tested. The efficacy of bisphosphonate was at best equivocal. CONCLUSION: The progression of CA is unpredictable and treatments effective against GSD, such as bisphosphonates and radiotherapy, have proved ineffective for this condition. New treatments are thus urgently required.
[Mh] Termos MeSH primário: Angiomatose/diagnóstico
Cistos Ósseos/diagnóstico
Doenças Ósseas/diagnóstico
Diagnóstico por Imagem
[Mh] Termos MeSH secundário: Adulto
Diagnóstico Diferencial
Feminino
Seres Humanos
Masculino
Meia-Idade
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1702
[Cu] Atualização por classe:170224
[Lr] Data última revisão:
170224
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:161028
[St] Status:MEDLINE


  10 / 2441 MEDLINE  
              first record previous record
seleciona
para imprimir
Fotocópia
Texto completo
[PMID]:27721303
[Au] Autor:Christos PA; Triantafyllia KD; Prodromos HM; Ioannis KS
[Ad] Endereço:Department of Pathology, Faculty of Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.
[Ti] Título:Coexistence of breast carcinoma, pseudoangiomatous stromal hyperplasia, and neurofibromatosis type 1 in a male patient.
[So] Source:Indian J Pathol Microbiol;59(4):563-564, 2016 Oct-Dec.
[Is] ISSN:0974-5130
[Cp] País de publicação:India
[La] Idioma:eng
[Mh] Termos MeSH primário: Angiomatose/diagnóstico
Doenças Mamárias/diagnóstico
Neoplasias da Mama/diagnóstico
Carcinoma Ductal/diagnóstico
Hiperplasia/diagnóstico
Neurofibromatose 1/diagnóstico
[Mh] Termos MeSH secundário: Adulto
Angiomatose/complicações
Angiomatose/patologia
Antígenos CD34/análise
Biomarcadores Tumorais/análise
Biópsia
Doenças Mamárias/complicações
Doenças Mamárias/patologia
Neoplasias da Mama/patologia
Carcinoma Ductal/complicações
Carcinoma Ductal/patologia
Histocitoquímica
Seres Humanos
Hiperplasia/complicações
Hiperplasia/patologia
Imuno-Histoquímica
Masculino
Microscopia
Neurofibromatose 1/complicações
Neurofibromatose 1/patologia
Proteínas S100/análise
[Pt] Tipo de publicação:CASE REPORTS; LETTER
[Nm] Nome de substância:
0 (Antigens, CD34); 0 (Biomarkers, Tumor); 0 (S100 Proteins)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170313
[Lr] Data última revisão:
170313
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161011
[St] Status:MEDLINE
[do] DOI:10.4103/0377-4929.191773



página 1 de 245 ir para página                         
   


Refinar a pesquisa
  Base de dados : MEDLINE Formulário avançado   

    Pesquisar no campo  
1  
2
3
 
           



Search engine: iAH v2.6 powered by WWWISIS

BIREME/OPAS/OMS - Centro Latino-Americano e do Caribe de Informação em Ciências da Saúde