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Search Results - ARÁMBULA-MERAZ, E
Search Results - ARÁMBULA-MERAZ, E
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Glucose-6-phosphate dehydrogenase deficiency in northern Mexico and description of a novel mutation
by
GARCÍA-MAGALLANES, N.
,
LUQUE-ORTEGA, F.
,
AGUILAR-MEDINA, E. M.
,
RAMOS-PAYÁN, R.
,
GALAVIZ-HERNÁNDEZ, C.
,
ROMERO-QUINTANA, J. G.
,
DEL POZO-YAUNER, L.
,
RANGEL-VILLALOBOS, H.
,
ARÁMBULA-MERAZ, E.
Published in
Journal of genetics
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Glucose-6-phosphate dehydrogenase (G6PD) molecular variant deficiency: Identification in Panama pediatric population
by
Cossio – Gurrola, G.
,
Arámbula – Meraz, E.
,
Perea, M.
,
García, N.
,
Correa, A. Samudio
,
Rueda, K.
,
Chial, M.
Published in
Blood cells, molecules, & diseases
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Parasitaemia levels in Plasmodium chabaudi infected-mice modify IFN-γ and IL-10 expression after a homologous or heterologous challenge
by
AGUILAR-MEDINA, M
,
RAMOS-PAYÁN, R
,
ARÁMBULA-MERAZ, E
,
SÁNCHEZ-TORRES, L
,
FAVILA-CASTILLO, L
Published in
Parasite immunology
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DNA sequencing analysis of several G6PD variants previously defined by PCR-restriction enzyme analysis
by
Vaca, Gerardo
,
Arámbula Meraz, Eliakym
Published in
Genetics and molecular biology
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Parasitaemia levels in Plasmodium chabaudi infected-mice modify IFN-g and IL-10 expression after a homologous or heterologous challenge
by
Aguilar-Medina, M
,
Ramos-Payan, R
,
Arambula-Meraz, E
,
Sanchez-Torres, L
,
Favila-Castillo, L
Published in
Parasite immunology
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Identification of novel mutation in cathepsin C gene causing Papillon-Lefèvre Syndrome in Mexican patients
by
Romero-Quintana, José G
,
Frías-Castro, Luis O
,
Arámbula-Meraz, Eliakym
,
Aguilar-Medina, Maribel
,
Dueñas-Arias, Jesús E
,
Melchor-Soto, Jesús D
,
Romero-Navarro, José G
,
Ramos-Payán, Rosalío
Published in
BMC genetics
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47,XXY/48,XXXY/49,XXXXY mosaic with hydrocephaly: a case report and review of the literature
by
Dueñas-Arias, Jesús E
,
Aguilar-Medina, Maribel
,
Arámbula-Meraz, Eliakym
,
Valenzuela-Camacho, Juliana B
,
Vega-Solano, Angelina
,
Granados, Julio
,
Ramos-Payán, Rosalío
Published in
Journal of medical case reports
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Tetralogy of Fallot associated with macrocephaly-capillary malformation syndrome: a case report and review of the literature
by
Dueñas-Arias, Jesus E
,
Arámbula-Meraz, Eliakym
,
Frías-Castro, Luis O
,
Ramos-Payán, Rosalio
,
Quibrera-Matienzo, Jose A
,
Luque-Ortega, Fred
,
Aguilar-Medina, E Maribel
Published in
Journal of medical case reports
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Tetralogy of Fallot associated with macrocephaly-capillary malformation syndrome: a case report and review of the literature
by
Dueñas-Arias, Jesus E
,
Arámbula-Meraz, Eliakym
,
Frías-Castro, Luis O
,
Ramos-Payán, Rosalio
,
Quibrera-Matienzo, Jose A
,
Luque-Ortega, Fred
,
Aguilar-Medina, E Maribel
Published in
Journal of medical case reports
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CO238. ASOCIACIÓN DE LA VARIANTE R55C EN EL GEN DE LA ADIPONECTINA CON ALTERACIONES RELACIONADAS A SÍNDROME METABÓLICO EN NIÑOS
by
Melissa de Jesús Vega Burgueño
,
Javier Abednego Magaña Gómez
,
Dalia Magaña Ordorica
,
Marcela de Jesús Vergara Jiménez
,
Mayra Arias Gastélum
,
Meráz, Eliakym Arámbula
,
Daniela Moreno Mascareño
Published in
Archivos latinoamericanos de nutrición
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