Amândio António Rocha Dias de Sousa


AuthID: R-000-0G8

Confirmed Publications: 79



61
TITLE: A novel mutation (Cys83Tyr) in the second zinc finger of NR2E3 in enhanced S-cone syndrome  Full Text
AUTHORS: Amandio Rocha Sousa ; Takaaki Hayashi; Nuno Lourenco Gomes; Susana Penas ; Elisete Brandao; Paulo Rocha; Mitsuyoshi Urashima; Hisashi Yamada; Hiroshi Tsuneoka; Fernando Falcao Reis ;
PUBLISHED: 2011, SOURCE: EVER Meeting in GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, VOLUME: 249, ISSUE: 2
INDEXED IN: Scopus WOS CrossRef: 9
IN MY: ORCID | CIÊNCIAVITAE
62
TITLE: Analyses of aqueous humour ghrelin levels of eyes with and without glaucoma
AUTHORS: Rocha Sousa, A ; Alves Faria, P; Falcao Pires, I ; Falcao Reis, F ; Leite Moreira, AF ;
PUBLISHED: 2009, SOURCE: BRITISH JOURNAL OF OPHTHALMOLOGY, VOLUME: 93, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 10
IN MY: ORCID | CIÊNCIAVITAE
63
TITLE: ETB2 Receptor Subtype Stimulation Relaxes the Iris Sphincter Muscle
AUTHORS: Rocha Sousa, A ; Saraiva, J; Amaral, M; Alves Faria, P; Falcao Reis, F ; Leite Moreira, AF ;
PUBLISHED: 2009, SOURCE: PHYSIOLOGICAL RESEARCH, VOLUME: 58, ISSUE: 6
INDEXED IN: Scopus WOS
IN MY: ORCID | CIÊNCIAVITAE
64
TITLE: Cardiac, skeletal, and smooth muscle regulation by ghrelin
AUTHORS: Adelino F Leite Moreira ; Amandio Rocha Sousa ; Tiago Henriques Coelho ;
PUBLISHED: 2008, SOURCE: VITAMINS AND HORMONES, GHRELIN, VOLUME: 77
INDEXED IN: Scopus WOS CrossRef: 18
IN MY: ORCID | CIÊNCIAVITAE
65
TITLE: The obestatin/ghrelin system as a novel regulatory mechanism of iris muscle contraction  Full Text
AUTHORS: Rocha Sousa, A ; Falcao Reis, F ; Leite Moreira, AF ;
PUBLISHED: 2008, SOURCE: CURRENT EYE RESEARCH, VOLUME: 33, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID | CIÊNCIAVITAE
66
TITLE: Potential role of the growth hormone secretagogues in clinical practice
AUTHORS: Amandio Rocha Sousa ; Tiago Henriques Coelho ; Adelino F Leite Moreira ;
PUBLISHED: 2007, SOURCE: EXPERT OPINION ON THERAPEUTIC PATENTS, VOLUME: 17, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID | CIÊNCIAVITAE
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TITLE: Identification of XLRS1 gene mutation (608C > T) in a Portuguese family with juvenile retinoschisis
AUTHORS: Teixeira, C ; Rocha Sousa, A ; Trump, D; Brandao, E; Falcao Reis, F ;
PUBLISHED: 2005, SOURCE: Congress of the European-Association-for-Vision-and-Research (EVER 2004) in EUROPEAN JOURNAL OF OPHTHALMOLOGY, VOLUME: 15, ISSUE: 5
INDEXED IN: Scopus WOS CrossRef: 3
IN MY: ORCID | CIÊNCIAVITAE
Page 7 of 8. Total results: 79.

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