Results 1 to 10 of about 152 (75)
A study on nine strains of T. cruzi isolated from man, from animais and from triatomine bugs in Brazil are described. The parasites were slightly viscerotropic in white mice in six of the strains, highly viscerotropic and cardiotropic in two strains, and
W. B. Petana, J. R. Coura
doaj
Objetivo. Determinar frecuencias genotípicas y alélicas de los polimorfismos +138/ex1I/D A del gen de ET-1 (138 ex1 I/D) y el polimorfismo H323H(C/T) del gen del receptor A de ET-1(H323H RAET-1) en mujeres pre y posmenopáusicas, con el objeto de ...
Oscar Lassen +6 more
doaj +2 more sources
Caso 5: homem de 40 anos de idade, hipertenso, que apresentou dor abdominal e choque
Diego R. Barbosa Pereira +2 more
doaj +1 more source
Tuberculosis miliar con compromiso cardiaco en el puerperio inmediato: presentación de un caso
La tuberculosis miliar es una forma de enfermedad progresiva, resultante de la diseminación del Mycobacterium tuberculosis. Afecta a niños, ancianos y a inmunodeprimidos.
Geovedy Martínez García +2 more
doaj
Congenital Hypertrophy of Heart ? (Cardiomegalia Glycogenica): Specimen [PDF]
openaire +2 more sources
Derrame pleural bilateral en pacientes sin insuficiencia cardiaca
Fundamento: el derrame pleural es una enfermedad frecuente en la clínica, a la que debe enfrentarse no sólo el internista y el neumólogo, sino otros especialistas incluyendo al médico general.
Rafael Pila Pérez +2 more
doaj
Síndrome do PRKAG2: É Efetivo o Rastreio com Ecocardiograma Precoce em Crianças com Genótipo Positivo? [PDF]
Maria Elisa Lucena Sales de Melo Assunção +2 more
doaj +1 more source
Case 4 - A 79-Year-Old Man with Congestive Heart Failure Due to Restrictive Cardiomyopathy
Sumaia Mustafa +5 more
doaj +1 more source
CARDIOMEGALIA COMO INDICADOR PROGNÓSTICO NA INSUFICIÊNCIA CARDÍACA: uma revisão sistemática
Porfirio da Silva Junior, Rogerio +7 more
openaire +2 more sources
Some of the next articles are maybe not open access.
Pathology Research and Practice, 1986
Glycogen storage disease type II Pompe (GSD II) is a lysosomal storage disease caused by an inherited deficiency of acid alpha-glucosidase. In addition to the classical infantile form of GSD II, several clinical variants are known. We describe an infant with the classical course of the disease. Our patient differs from the classical variant by the lack
K Ullrich, H Grobe
exaly +3 more sources
Glycogen storage disease type II Pompe (GSD II) is a lysosomal storage disease caused by an inherited deficiency of acid alpha-glucosidase. In addition to the classical infantile form of GSD II, several clinical variants are known. We describe an infant with the classical course of the disease. Our patient differs from the classical variant by the lack
K Ullrich, H Grobe
exaly +3 more sources

