Results 121 to 130 of about 2,967 (173)

Venous thromboembolism in women: new challenges for an old disease. [PDF]

J Vasc Bras, 2020
de Oliveira ALML, Paschôa AF, Marques MA.   +2 more
europepmc   +1 more source

Myopathy due to carnitine palmitoyltransferase II deficiency: updating genetic aspects of the first publication in Brazil. [PDF]

Arq Neuropsiquiatr
Lorenzoni PJ, Kay CSK, Ducci RD, Fustes OJH, Rodrigues PRDVP, Arndt RC, Scola RH, Werneck LC.   +7 more
europepmc   +1 more source

Profilaxia de tromboembolismo venoso na gestação. [PDF]

J Vasc Bras, 2016
de Oliveira ALML, Marques MA.
europepmc   +1 more source

Incidence of variant hemoglobins in newborns attended by a public health laboratory. [PDF]

Einstein (Sao Paulo), 2018
Reis FMS, Branco RROC, Conceição AM, Trajano LPB, Vieira JFPDN, Ferreira PRB, Araújo ÉJF.   +6 more
europepmc   +1 more source

Sporadic Kindler syndrome with a novel mutation. [PDF]

An Bras Dermatol, 2013
Almeida HL, Heckler GT, Fong K, Lai-Cheong J, McGrath J.   +4 more
europepmc   +1 more source

Loss of Imprinting of IGF2 and H19, Promoter Usage of IGF2, Loss of Heterozigosity of IGF2R and Helicobacter pylori Infection in Laryngeal Squamous Cell Carcinoma (LSCC)

, 2006
The imprinted gene IGF2 codes for the mitogenic peptide, comprising 67 amino acids and contributing to tumor growth through its autocrine or endocrine effects. Its expression, directed from four different promoters, is regulated on the level of DNA methylation, since it is reciprocally imprinted with H19.
Gall Trošelj, Koraljka, Grbeša, Ivana
openaire   +1 more source

Myosin-binding Protein C Compound Heterozygous Variant Effect on the Phenotypic Expression of Hypertrophic Cardiomyopathy. [PDF]

Arq Bras Cardiol, 2017
Rafael JF, Cruz FEDS, Carvalho ACC, Gottlieb I, Cazelli JG, Siciliano AP, Dias GM.   +6 more
europepmc   +1 more source

Double heterozigosity HbE/alpha-thalassemia in a Cambodian child.

Haematologica, 1986
P, Perutelli, A, Schenone, F, Scuderi
openaire   +1 more source