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Wyszukujesz frazę ""Corona‐Rivera, Alfredo"" wg kryterium: Autor


Wyświetlanie 1-6 z 6
Tytuł :
Complete blood count differences in a cohort of Down syndrome neonates with transient abnormal myelopoiesis screened for GATA1 pathogenic variants.
Autorzy :
Orozco-Vela M; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.
Corona-Rivera A; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Cruz-Osorio RM; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Mendoza-Maldonado L; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Márquez-Mora A; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Barba-Barba CC; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics, Service of Genetics, Center for Registry and Research on Congenital Anomalies (CRIAC), Guadalajara, Jalisco, Mexico.
Baldomero-López A; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics, Service of Genetics, Center for Registry and Research on Congenital Anomalies (CRIAC), Guadalajara, Jalisco, Mexico.
Bobadilla-Morales L; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Corona-Rivera JR; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics, Service of Genetics, Center for Registry and Research on Congenital Anomalies (CRIAC), Guadalajara, Jalisco, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Sep; Vol. 182 (9), pp. 2085-2093. Date of Electronic Publication: 2020 Jul 18.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*blood
GATA1 Transcription Factor/*genetics
Leukemoid Reaction/*blood
Adult ; Blood Cell Count ; Down Syndrome/genetics ; Down Syndrome/pathology ; Female ; Humans ; Infant ; Infant, Newborn ; Leukemoid Reaction/genetics ; Leukemoid Reaction/pathology ; Male ; Middle Aged ; Mutation/genetics
SCR Disease Name :
Myeloproliferative Syndrome, Transient
Czasopismo naukowe
Tytuł :
Maternal risk factors for congenital heart defects in infants with Down syndrome from Western Mexico.
Autorzy :
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Nieto-García R; Service of Cardiology, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Gutiérrez-Chávez AS; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Rios-Flores IM; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Fabián-Morales GE; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Zavala-Cortés I; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Lugo-Iglesias C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Sep; Vol. 179 (9), pp. 1857-1865. Date of Electronic Publication: 2019 Jul 19.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*epidemiology
Heart Defects, Congenital/*epidemiology
Heart Septal Defects/*epidemiology
Heart Septal Defects, Atrial/*epidemiology
Adult ; Down Syndrome/complications ; Down Syndrome/physiopathology ; Female ; Heart Defects, Congenital/complications ; Heart Defects, Congenital/physiopathology ; Heart Septal Defects/complications ; Heart Septal Defects/physiopathology ; Heart Septal Defects, Atrial/complications ; Heart Septal Defects, Atrial/physiopathology ; Humans ; Infant ; Male ; Maternal Age ; Mexico/epidemiology ; Paternal Age ; Pregnancy ; Risk Factors ; United States/epidemiology
SCR Disease Name :
Atrioventricular Septal Defect
Czasopismo naukowe
Tytuł :
Prevalence and risk factors for Down syndrome: A hospital-based single-center study in Western Mexico.
Autorzy :
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Martínez-Macías FJ; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Rios-Flores IM; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Flores-Guevara PA; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Orozco-Vela M; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Aranda-Sánchez CI; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Brukman-Jiménez SA; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Mar; Vol. 179 (3), pp. 435-441. Date of Electronic Publication: 2019 Jan 21.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*epidemiology
Adolescent ; Adult ; Case-Control Studies ; Down Syndrome/etiology ; Female ; Humans ; Male ; Maternal Exposure/adverse effects ; Mexico/epidemiology ; Middle Aged ; Odds Ratio ; Pregnancy ; Prevalence ; Risk Assessment ; Risk Factors ; Young Adult
Czasopismo naukowe
Tytuł :
Descriptive study of the complete blood count in newborn infants with Down syndrome.
Autorzy :
Martínez-Macías FJ; Department of Molecular Biology and Genomics, Dr. Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara, Health Sciences University Center, Guadalajara, Jalisco, México.
Bobadilla-Morales L; Department of Molecular Biology and Genomics, Dr. Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara, Health Sciences University Center, Guadalajara, Jalisco, México.; Center for Registry and Research in Congenital Anomalies (CRIAC), Pediatrics Division, Service of Genetics and Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
González-Cruz J; Pediatrics Division, Service of Neonatology, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
Quiles-Corona M; Pediatrics Division, Service of Neonatology, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
Corona-Rivera A; Department of Molecular Biology and Genomics, Dr. Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara, Health Sciences University Center, Guadalajara, Jalisco, México.; Center for Registry and Research in Congenital Anomalies (CRIAC), Pediatrics Division, Service of Genetics and Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Pediatrics Division, Service of Genetics and Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
Orozco-Vela M; Department of Molecular Biology and Genomics, Dr. Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara, Health Sciences University Center, Guadalajara, Jalisco, México.
Silva-Cruz R; Department of Molecular Biology and Genomics, Dr. Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara, Health Sciences University Center, Guadalajara, Jalisco, México.
Velarde-Rivera F; Central Laboratory, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
Corona-Rivera JR; Department of Molecular Biology and Genomics, Dr. Enrique Corona-Rivera Institute of Human Genetics, University of Guadalajara, Health Sciences University Center, Guadalajara, Jalisco, México.; Center for Registry and Research in Congenital Anomalies (CRIAC), Pediatrics Division, Service of Genetics and Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, México.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2017 Apr; Vol. 173 (4), pp. 897-904. Date of Electronic Publication: 2017 Feb 07.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*blood
Hematologic Diseases/*blood
Lymphocytosis/*blood
Polycythemia/*blood
Thrombocytopenia/*blood
Blood Cell Count ; Case-Control Studies ; Down Syndrome/complications ; Down Syndrome/diagnosis ; Early Diagnosis ; Erythrocyte Indices ; Erythrocytes, Abnormal ; Gestational Age ; Hematologic Diseases/complications ; Hematologic Diseases/diagnosis ; Humans ; Infant ; Infant, Newborn ; Logistic Models ; Lymphocytosis/complications ; Lymphocytosis/diagnosis ; Odds Ratio ; Polycythemia/complications ; Polycythemia/diagnosis ; Prospective Studies ; Thrombocytopenia/complications ; Thrombocytopenia/diagnosis
SCR Disease Name :
Macrocytosis, Familial
Czasopismo naukowe
    Wyświetlanie 1-6 z 6

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