Results 111 to 120 of about 3,010 (189)

Syncope as a Phenotypic Expression of Hereditary Transthyretin Amyloidosis Val142Ile (Val122Ile). [PDF]

Arq Bras Cardiol, 2020
Nunes NSV, Carvalho JPM, Costa FS, Nacif MS, Dominato J, Mesquita CT, Mesquita ET.   +6 more
europepmc   +1 more source

Manutenção e multiplicação de cultivares e sementes genéticas de algodoeiro. [PDF]

, 2011
Taxa de cruzamento natural em algodoeiro.bitstream/CNPA/15110/1/CIRTEC45 ...
CARVALHO, L. P. de
core  

Relevance of loss of heterozigosity in chromosome 3p in non small cell lung carcinoma as prognostic factor

, 1999
Recent advances on carcinogenesis have led to the recognition of different patterns of behaviour of non-small cell lung cancers appart from those guided by the TNM staging system and the histologic subtype. The frequent genetic loss on chromosome 3p in all kinds of lung carcinoma leads to the suspect of the presence of a tumor suppresor gene located in
Maestro, María Luisa, Izquierdo, Luis Ángel, Sánchez-Pernaute, Andrés, Sanz Casla, María Teresa, González, Sonia, Torres, Antonio José, Barco, Victoria del, Autrán Gómez, Ana María, Pérez Aguirre, Elia, Balibrea, Jose Luis   +9 more
openaire   +1 more source

Mutações no gene da metilenotetrahidrofolato redutase e síndrome de Down

Cadernos de Saúde Pública, 2002
Sindrome de Down (SD) é uma alteração genética e metabólica complexa atribuída à presença de três cópias do cromossomo 21. O cromossomo extra em 93% dos casos é de origem materna e é resultante de uma segregação anormal durante a meiose (não-disjunção ...
Grillo Laura Brunelli das Neves, Acácio Gregório Lorenzo, Barini Ricardo, Pinto Jr. Walter, Bertuzzo Carmen Silvia   +4 more
doaj  

Molecular study of hearing loss in Minas Gerais, Brazil. [PDF]

Braz J Otorhinolaryngol, 2020
Schüffner ROA, Nascimento KL, Dias FA, Silva PHTD, Pires WGB, Cipriano NM, Santos LLD.   +6 more
europepmc   +1 more source

Update of the Brazilian Guideline for Familial Hypercholesterolemia - 2021. [PDF]

Arq Bras Cardiol, 2021
Izar MCO, Giraldez VZR, Bertolami A, Santos Filho RDD, Lottenberg AM, Assad MHV, Saraiva JFK, Chacra APM, Martinez TLR, Bahia LR, Fonseca FAH, Faludi AA, Sposito AC, Chagas ACP, Jannes CE, Amaral CK, Araújo DB, Cintra DE, Coutinho EDR, Cesena F, Xavier HT, Mota ICP, Giuliano ICB, Faria Neto JR, Kato JT, Bertolami MC, Miname MH, Castelo MHCG, Lavrador MSF, Machado RM, Souza PG, Alves RJ, Machado VA, Salgado Filho W.   +33 more
europepmc   +1 more source

Phenotypic Variability in a Family with Andersen-Tawil Syndrome. [PDF]

Arq Bras Cardiol
Nascimento SUCND, Duarte JOP, Magalhães LP, Guabiru AT, Santos AS, Cavalvanti E, Rodrigues VB, Aras R.   +7 more
europepmc   +1 more source

Apical Sparing and Granular Sparkling: Not Everything that Glitters Is Cardiac Amyloidosis. [PDF]

Arq Bras Cardiol
Barros APM, Romero CE, Cardoso JN, Fernandes F, Hotta VT.   +4 more
europepmc   +1 more source

Unveiling the Genetic Puzzle: Asymmetric Hypertrophy in a Heart Transplant Recipient Linked to Birt-Hogg-Dubé Syndrome. [PDF]

Arq Bras Cardiol
Furquim SR, Pires LVL, Buriti NA, Carvalho MLP, Marques EL, Linnenkamp BDW, Sacilotto L, Marcondes-Braga FG, Campos IW, Seguro LFBDC, Mangini S, Avila MS, Bacal F, Krieger JE.   +13 more
europepmc   +1 more source