Jose Leopoldo de Melo Castro: Cardiologista

Jose Leopoldo de Melo Castro

CRM 9664 MG

Cardiologista

Locais de atendimento

Penha

LOCALIZAÇÃO

Avenida Joao Soares Silva, 101 / C - Penha, Itabira - MG

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ESPECIALIDADES ATENDIDAS

Cardiologista

CONTATO

Especialidades
Publicações
  • Castro JL, Kim MK, Char DH, Saunders WM, Chen GT, Stone RD. NEOVASCULAR GLAUCOMA AFTER HELIUM ION IRRADIATION FOR UVEAL MELANOMA. 01 de Fevereiro de 1986.
  • Castro JL, Cabrera R. [HEMATOPOIESIS AND LIVER CIRRHOSIS]. 01 de Janeiro de 1970.
  • Castro JL, Gottlieb F. PERFORATION OF THE GLOBE DURING STRABISMUS SURGERY. 01 de Agosto de 1970.
  • Castro JL, Bianciotti LG, Vatta MS, Dominguez AE, Vescina C, Magariños J, et al. QUANTITATIVE MODIFICATIONS INDUCED BY ANGIOTENSIN II ON RAT BILE SECRETION. 01 de Dezembro de 1994.
  • Castro JL, Baker R, Guiblin AR, Hobbs SC, Jenkins MR, Russell MG, et al. SYNTHESIS AND BIOLOGICAL ACTIVITY OF 3-[2-(DIMETHYLAMINO)ETHYL]-5-[(1,1-DIOXO-5-METHYL-1,2,5-THIADIAZOLIDIN- 2-YL)-METHYL]-1H-INDOLE AND ANALOGUES: AGONISTS FOR THE 5-HT1D RECEPTOR. 01 de Setembro de 1994.
  • Castro JL, Street LJ, Baker R, Chambers MS, Guiblin AR, Hobbs SC, et al. SYNTHESIS AND SEROTONERGIC ACTIVITY OF 5-(OXADIAZOLYL)TRYPTAMINES: POTENT AGONISTS FOR 5-HT1D RECEPTORS. 01 de Maio de 1993.
  • Castro JL, Campa F, Pino E, Mula F, Caro JA, Martínez O. [THE CRITICAL RECORD: THE REGISTRY SYSTEM IN CONSULTATION ON DEMAND]. 01 de Maio de 1993.
  • Castro JL, Ball RG, Broughton HB, Russell MG, Rathbone D, Watt AP, et al. CONTROLLED MODIFICATION OF ACIDITY IN CHOLECYSTOKININ B RECEPTOR ANTAGONISTS: N-(1,4-BENZODIAZEPIN-3-YL)-N'-[3-(TETRAZOL-5-YLAMINO) PHENYL]UREAS. 01 de Fevereiro de 1996.
  • Castro JL, Broughton HB, Russell MG, Rathbone D, Watt AP, Ball RG, et al. 5-(PIPERIDIN-2-YL)- AND 5-(HOMOPIPERIDIN-2-YL)-1,4-BENZODIAZEPINES: HIGH-AFFINITY, BASIC LIGANDS FOR THE CHOLECYSTOKININ-B RECEPTOR. 01 de Agosto de 1997.
  • Castro JL, Street LJ, Guiblin AR, Jelley RA, Russell MG, Sternfeld F, et al. 3-[2-(PYRROLIDIN-1-YL)ETHYL]INDOLES AND 3-[3-(PIPERIDIN-1-YL)PROPYL]INDOLES: AGONISTS FOR THE H5-HT1D RECEPTOR WITH HIGH SELECTIVITY OVER THE H5-HT1B SUBTYPE. 01 de Outubro de 1997.

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