Alberto Manuel Barros da Silva


AuthID: R-000-KE6

Confirmed Publications: 266



221
TITLE: High frequency of DAZ1/DAZ2 gene deletions in patients with severe oligozoospermia
AUTHORS: Fernandes, S; Huellen, K; Goncalves, J ; Dukal, H; Zeisler, J; De MEyts, ER; Skakkebaek, NE; Habermann, B; Krause, W; Sousa, M ; Barros, A ; Vogt, PH;
PUBLISHED: 2002, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 8, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 115
IN MY: ORCID | ResearcherID
222
TITLE: Predictive value of testicular histology in secretory azoospermic subgroups and clinical outcome after microinjection of fresh and frozen-thawed sperm and spermatids
AUTHORS: Sousa, M ; Cremades, N; Silva, J; Oliveira, C; Ferraz, L; da Silva, JT; Viana, P; Barros, A ;
PUBLISHED: 2002, SOURCE: HUMAN REPRODUCTION, VOLUME: 17, ISSUE: 7
INDEXED IN: Scopus WOS CrossRef: 91
IN MY: ORCID | ResearcherID
223
TITLE: Preimplantation genetic diagnosis using FISH for carriers of Robertsonian translocations: the Portuguese experience  Full Text
AUTHORS: Alves, C; Sousa, M ; Silva, J; Barros, A ;
PUBLISHED: 2002, SOURCE: PRENATAL DIAGNOSIS, VOLUME: 22, ISSUE: 12
INDEXED IN: Scopus WOS CrossRef: 19
IN MY: ORCID | ResearcherID
224
TITLE: Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies  Full Text
AUTHORS: Alves, C; Carvalho, F ; Cremades, N; Sousa, M ; Barros, A ;
PUBLISHED: 2002, SOURCE: EUROPEAN JOURNAL OF HUMAN GENETICS, VOLUME: 10, ISSUE: 8
INDEXED IN: Scopus WOS CrossRef: 43
IN MY: ORCID | ResearcherID
225
TITLE: Characterization by FISH analysis of the chromosome complement of immature and in-vitro-matured human oocytes
AUTHORS: Cremades, N; Alves, C; Silva, J; Bernabeu, R; Barros, A ; Sousa, M ;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
INDEXED IN: WOS
IN MY: ResearcherID
226
TITLE: Developmental potential of elongating and elongated spermatids obtained after in-vitro maturation of isolated round spermatids
AUTHORS: Cremades, N; Sousa, M ; Bernabeu, R; Barros, A ;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef: 42
IN MY: ORCID | ResearcherID
227
228
TITLE: High deletion frequency of the complete AZFa sequence in men with Sertoli-cell-only syndrome
AUTHORS: Kamp, C; Huellen, K; Fernandes, S; Sousa, M ; Schlegel, PN; Mielnik, A; Kleiman, S; Yavetz, H; Krause, W; Kupker, W; Johannisson, R; Schulze, W; Weidner, W; Barros, A ; Vogt, PH;
PUBLISHED: 2001, SOURCE: MOLECULAR HUMAN REPRODUCTION, VOLUME: 7, ISSUE: 10
INDEXED IN: Scopus WOS CrossRef: 116
IN MY: ORCID | ResearcherID
229
TITLE: Molecular analysis of the complexity of the DAZ gene family in AZFc reveals partial DAZ deletions in men with severe oligozoospermia as novel mutation event
AUTHORS: Fernandes, S; Goncalves, J; Ditton, HJ; Huellen, K; Sousa, M; Barros, A ; Vogt, PH;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
INDEXED IN: WOS
IN MY: ResearcherID
230
TITLE: Population screening of Y-chromosome microdeletions in Portugal: a study involving 428 infertile male patients
AUTHORS: Barros, A ; Carvalho, F ; Fernandes, S; Torgal, A; Silva, J; Sousa, M;
PUBLISHED: 2001, SOURCE: HUMAN REPRODUCTION, VOLUME: 16
INDEXED IN: WOS
IN MY: ResearcherID
Página 23 de 27. Total de resultados: 266.

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