321
TITLE: Recent advances in the molecular pathology of familial amyloid polyneuropathy  Full Text
AUTHORS: Saraiva, MJM ;
PUBLISHED: 1991, SOURCE: Neuromuscular Disorders, VOLUME: 1, ISSUE: 1
INDEXED IN: Scopus
IN MY: ORCID
322
TITLE: REPORT OF AN HETEROZYGOTIC INDIVIDUAL FOR 2 TRANSTHYRETIN VARIANTS
AUTHORS: ALVES, IL; ALMEIDA, MR ; ALTLAND, K; PALHA, JA; COELHO, T; COSTA, PP; SARAIVA, MJM ;
PUBLISHED: 1991, SOURCE: AMERICAN JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 4
INDEXED IN: WOS
323
TITLE: STUDIES ON THE SYNTHESIS AND SECRETION OF TRANSTHYRETIN BY THE HUMAN HEPATOMA-CELL LINE HEP G2  Full Text
AUTHORS: BLANER, WS; BONIFACIO, MJ; FELDMAN, HD; PIANTEDOSI, R; SARAIVA, MJM ;
PUBLISHED: 1991, SOURCE: FEBS LETTERS, VOLUME: 287, ISSUE: 1-2
INDEXED IN: Scopus WOS CrossRef: 12
324
TITLE: TRANSTHYRETIN LEU-68 IN A FORM OF CARDIAC AMYLOIDOSIS
AUTHORS: ALMEIDA, MR ; HESSE, A; STEINMETZ, A; MAISCH, B; ALTLAND, K; LINKE, RP; GAWINOWICZ, MA; SARAIVA, MJM ;
PUBLISHED: 1991, SOURCE: BASIC RESEARCH IN CARDIOLOGY, VOLUME: 86, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 32
325
TITLE: CARDIAC AMYLOIDOSIS - REPORT OF A PATIENT HETEROZYGOUS FOR THE TRANSTHYRETIN ISOLEUCINE 122 VARIANT
AUTHORS: SARAIVA, MJM ; SHERMAN, W; MARBOE, C; FIGUEIRA, A; COSTA, P; DEFREITAS, AF; GAWINOWICZ, MA;
PUBLISHED: 1990, SOURCE: SCANDINAVIAN JOURNAL OF IMMUNOLOGY, VOLUME: 32, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 31
326
TITLE: HAPLOTYPE ANALYSIS OF DIFFERENT FAP INDIVIDUALS WITH METHIONINE-30 MUTATION IN EUROPE
AUTHORS: ALMEIDA, MD; SASAKI, H; SAKAKI, Y; SALVI, F; FERLINI, A; COSTA, PP; SARAIVA, MJ ;
PUBLISHED: 1990, SOURCE: 1ST SYMP ON FAMILIAL AMYLOIDOTIC POLYNEUROPATHY AND OTHER TRANSTHYRETIN RELATED DISORDERS in FAMILIAL AMYLOIDOTIC POLYNEUROPATHY AND OTHER TRANSTHYRETIN RELATED DISORDERS
INDEXED IN: WOS
327
TITLE: PRENATAL-DIAGNOSIS OF FAMILIAL AMYLOIDOTIC POLYNEUROPATHY - EVIDENCE FOR AN EARLY EXPRESSION OF THE ASSOCIATED TRANSTHYRETIN METHIONINE-30
AUTHORS: ALMEIDA, MR ; ALVES, IL; SAKAKI, Y; COSTA, PP; SARAIVA, MJM ;
PUBLISHED: 1990, SOURCE: HUMAN GENETICS, VOLUME: 85, ISSUE: 6
INDEXED IN: WOS
328
TITLE: A NEW MUTATION CAUSING FAMILIAL AMYLOIDOTIC POLYNEUROPATHY  Full Text
AUTHORS: SKARE, JC; SARAIVA, MJM ; ALVES, IL; SKARE, IB; MILUNSKY, A; COHEN, AS; SKINNER, M;
PUBLISHED: 1989, SOURCE: BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, VOLUME: 164, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 27
329
TITLE: ACTIVITY OF A METALLOTHIONEIN-TRANSTHYRETIN FUSION GENE IN TRANSGENIC MICE - POSSIBLE EFFECT OF PLASMID SEQUENCES ON TISSUE-SPECIFIC EXPRESSION
AUTHORS: SASAKI, H; NAKAZATO, M; SARAIVA, MJM ; MATSUO, H; SAKAKI, Y;
PUBLISHED: 1989, SOURCE: MOLECULAR BIOLOGY & MEDICINE, VOLUME: 6, ISSUE: 4
INDEXED IN: Scopus WOS
330
TITLE: Haplotype analysis of familial amyloidotic polyneuropathy. Evidence for multiple origins of the Val?Met mutation most common to the disease
AUTHORS: Katsuji Yoshioka; Hirokazu Furuya; Hiroyuki Sasaki; Maria Joao Mascarenhas Saraiva ; Pedro P Costa; Yoshiyuki Sakaki;
PUBLISHED: 1989, SOURCE: Hum Genet - Human Genetics, VOLUME: 82, ISSUE: 1
INDEXED IN: CrossRef: 59
IN MY: ORCID
Page 33 of 36. Total results: 354.