Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Paulina Bravo J"'
Publikováno v:
Andes pediatrica : revista Chilena de pediatria. 92(3)
Prader-Willi Syndrome (PWS) is the most common cause of genetic obesity. Hyperphagia and obe sity are the most associated concepts with this condition. However, undernutrition secondary to severe hypotonia and feeding difficulties is the predominant
Publikováno v:
Andes Pediatrica. 92:359
Introduction Prader-Willi Syndrome (PWS) is the most common cause of genetic obesity. Hyperphagia and obe sity are the most associated concepts with this condition. However, undernutrition secondary to severe hypotonia and feeding difficulties is the
Publikováno v:
Revista chilena de pediatria. 89(3)
Cow's milk protein allergy (CMPA) is a common disease with a prevalence of 2-7%, increasingly so. It is characterized by an allergic reaction to one or more cow's milk proteins. There are not pathog nomonic clinical symptoms, and these will depend on
Autor:
Paulina Bravo J.
Publikováno v:
Andes Pediatrica. 90:690
Autor:
PAULINA BRAVO J, M. ISABEL HODGSON B
Publikováno v:
Revista chilena de pediatría. 82:87-92
Los trastornos de la alimentacion en el lactante y preescolar siguen siendo un motivo frecuente de consulta en policlinicos de pediatria y nutricion infantil. Descartar causas organicas, sobre todo cuando existe compromiso nutricional, es de fundamen
Autor:
Paulina, Bravo J, Gabriela, Castro C H
Publikováno v:
Revista chilena de pediatria. 85(4)
Inborn metabolic disorders are genetic diseases which are uncommon each one, but together they are not. They are characterized by an enzimatic defect that blocks a metabolic pathway, producing specific signs and symptoms. The current article pretends
Autor:
Gabriela Castro Ch, Paulina Bravo J
Publikováno v:
Revista chilena de pediatría v.85 n.4 2014
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Los errores congénitos del metabolismo son enfermedades genéticas poco frecuentes pero que en conjunto no lo son. Se caracterizan por un defecto enzimático que bloquea una vía metabólica produciendo manifestaciones clínicas características. El
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3890112f75aa400ef32f7e378362df5
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062014000400003
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062014000400003
Publikováno v:
Revista chilena de pediatría v.85 n.3 2014
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Hematological and neurological compromise due to vitamin B12 deficit in infant of a vegetarian mother: case report introduction : Vitamin B12 deficiency is extremely common in strict vegetarians and their variants. Infants of vegetarian mothers have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90b280dc792d7e7b0bb1fe96e5fb78be
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062014000300010
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0370-41062014000300010
Publikováno v:
Revista chilena de pediatria. 85(3)
Vitamin B12 deficiency is extremely common in strict vegetarians and their variants. Infants of vegetarian mothers have a higher risk of deficiency and are more prone to its effects.To report a case in order to warn people about the importance of sus
Publikováno v:
Revista chilena de pediatría. 73