Maria Clara Pereira de Sá Miranda
AuthID: R-000-ARA
111
TITLE: Nitroxidergic innervation of guinea pig cerebral arteries Full Text
AUTHORS: Barroso, CP; Edvinsson, L; Zhang, W; Sa, MCE; Springall, DR; Polak, JM; Gulbenkian, S;
PUBLISHED: 1996, SOURCE: JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, VOLUME: 58, ISSUE: 1-2
AUTHORS: Barroso, CP; Edvinsson, L; Zhang, W; Sa, MCE; Springall, DR; Polak, JM; Gulbenkian, S;
PUBLISHED: 1996, SOURCE: JOURNAL OF THE AUTONOMIC NERVOUS SYSTEM, VOLUME: 58, ISSUE: 1-2
112
TITLE: UNTITLED - REPLY
AUTHORS: MIRANDA, MCS;
PUBLISHED: 1995, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 18, ISSUE: 1
AUTHORS: MIRANDA, MCS;
PUBLISHED: 1995, SOURCE: JOURNAL OF INHERITED METABOLIC DISEASE, VOLUME: 18, ISSUE: 1
INDEXED IN: 
WOS
WOS113
TITLE: Prenatal diagnosis of GM2-gangliosidosis B1 variant
AUTHORS: Lemos, M; Pinto, R; Ribeiro, G; Ribeiro, H; Lopes, L; Sá C S Miranda;
PUBLISHED: 1995, SOURCE: Prenatal Diagnosis - Prenat. Diagn., VOLUME: 15, ISSUE: 6
AUTHORS: Lemos, M; Pinto, R; Ribeiro, G; Ribeiro, H; Lopes, L; Sá C S Miranda;
PUBLISHED: 1995, SOURCE: Prenatal Diagnosis - Prenat. Diagn., VOLUME: 15, ISSUE: 6
114
TITLE: Tay-Sachs disease: Intron 7 splice junction mutation in two Portuguese patients Full Text
AUTHORS: Maria G Ribeiro; Rui Pinto; Maria C Sa Miranda; Kunihiko Suzuki;
PUBLISHED: 1995, SOURCE: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, VOLUME: 1270, ISSUE: 1
AUTHORS: Maria G Ribeiro; Rui Pinto; Maria C Sa Miranda; Kunihiko Suzuki;
PUBLISHED: 1995, SOURCE: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, VOLUME: 1270, ISSUE: 1
INDEXED IN: 
CrossRef
CrossRef115
TITLE: The N370S mutation in the glucocerebrosidase gene of Portuguese type 1 Gaucher patients: Linkage to the PvuII polymorphism
AUTHORS: Lacerda, L; Amaral, O; Pinto, R; Aerts, J; S� Miranda, MC;
PUBLISHED: 1994, SOURCE: Journal of Inherited Metabolic Disease - J Inherit Metab Dis, VOLUME: 17, ISSUE: 1
AUTHORS: Lacerda, L; Amaral, O; Pinto, R; Aerts, J; S� Miranda, MC;
PUBLISHED: 1994, SOURCE: Journal of Inherited Metabolic Disease - J Inherit Metab Dis, VOLUME: 17, ISSUE: 1
116
TITLE: Role of pH in determining the cell-type-specific residual activity of glucocerebrosidase in type 1 Gaucher disease.
AUTHORS: van Weely, S; van den Berg, M; Barranger, JA; Sa Miranda, MC; Tager, JM; Aerts, JM;
PUBLISHED: 1993, SOURCE: Journal of Clinical Investigation - J. Clin. Invest., VOLUME: 91, ISSUE: 3
AUTHORS: van Weely, S; van den Berg, M; Barranger, JA; Sa Miranda, MC; Tager, JM; Aerts, JM;
PUBLISHED: 1993, SOURCE: Journal of Clinical Investigation - J. Clin. Invest., VOLUME: 91, ISSUE: 3
INDEXED IN: CrossRef
CrossRef117
TITLE: Echocardiographic assessment of interventricular septal defect corrected during the first year of life [Avaliação ecocardiográfica da comunicação interventricular corrigida no primeiro ano de vida.]
AUTHORS: Nascimento, R; Bastos, P; Torres, S; Campelo, M ; Pereira, M; de Sousa, AR; Van Zeller, P; Gomes, MR; Cunha, D;
PUBLISHED: 1992, SOURCE: Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology, VOLUME: 11, ISSUE: 4
AUTHORS: Nascimento, R; Bastos, P; Torres, S; Campelo, M ; Pereira, M; de Sousa, AR; Van Zeller, P; Gomes, MR; Cunha, D;
PUBLISHED: 1992, SOURCE: Revista portuguesa de cardiologia : orgao oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology, VOLUME: 11, ISSUE: 4
INDEXED IN: 
Scopus
Scopus118
TITLE: GAUCHER DISEASE TYPE-I - MOLECULAR AND BIOCHEMICAL-STUDIES IN 14 PORTUGUESE PATIENTS
AUTHORS: MIRANDA, MS; LACERDA, L; AMARAL, O; SANTOS, R; AERTS, H;
PUBLISHED: 1991, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 4
AUTHORS: MIRANDA, MS; LACERDA, L; AMARAL, O; SANTOS, R; AERTS, H;
PUBLISHED: 1991, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 4
INDEXED IN: WOS
WOS119
TITLE: GM2-gangliosidosis B1 variant: Analysis of β-hexosaminidase α gene mutations in 11 patients from a defined region in Portugal
AUTHORS: Dos Santos, MR; Tanaka, A; Sa Miranda, MC; Ribeiro, MG; Maia, M; Suzuki, K;
PUBLISHED: 1991, SOURCE: American Journal of Human Genetics, VOLUME: 49, ISSUE: 4
AUTHORS: Dos Santos, MR; Tanaka, A; Sa Miranda, MC; Ribeiro, MG; Maia, M; Suzuki, K;
PUBLISHED: 1991, SOURCE: American Journal of Human Genetics, VOLUME: 49, ISSUE: 4
INDEXED IN: Scopus
Scopus IN MY: 
ORCID
ORCID120
TITLE: The identification of type 1 Gaucher disease patients, asymptomatic cases and carriers in The Netherlands using urine samples: An evaluation Full Text
AUTHORS: Aerts, JMFG; Miranda, MCS; de Lacerda, LW; van Weely, S; Donker Koopman, W; Brouwer Kelder, B; Jansen, DC; van Leeuwen, M; Schram, AW; Tsiapara, A; Tager, JM;
PUBLISHED: 1991, SOURCE: Clinica Chimica Acta, VOLUME: 203, ISSUE: 2-3
AUTHORS: Aerts, JMFG; Miranda, MCS; de Lacerda, LW; van Weely, S; Donker Koopman, W; Brouwer Kelder, B; Jansen, DC; van Leeuwen, M; Schram, AW; Tsiapara, A; Tager, JM;
PUBLISHED: 1991, SOURCE: Clinica Chimica Acta, VOLUME: 203, ISSUE: 2-3
INDEXED IN: Scopus
Scopus IN MY: ORCID
ORCID