Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Ukraiński (UK)
Przejdź do strony domowej biblioteki Uniwersytet Ekonomiczny we Wrocławiu Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaUniwersytet Ekonomiczny we Wrocławiu

Wyszukujesz frazę ""Tauber KA"" wg kryterium: Autor

  Lista filtrów
Wyrównaj
    Wyświetlanie 1-4 z 4
    Tytuł:
    Cardiac arrest in a newborn: A case of pseudohypoaldosteronism.
    Autorzy:
    Tauber KA; Albany Medical Center Albany New York USA.
    Ermacor K; Albany Medical Center Albany New York USA.
    Listman J; Albany Medical Center Albany New York USA.
    Pokaż więcej
    Źródło:
    Clinical case reports [Clin Case Rep] 2024 Feb 09; Vol. 12 (2), pp. e8265. Date of Electronic Publication: 2024 Feb 09 (Print Publication: 2024).
    Typ publikacji:
    Case Reports
    Raport
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Novel variants in KAT6B spectrum of disorders expand our knowledge of clinical manifestations and molecular mechanisms.
    Autorzy:
    Yabumoto M; Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Kianmahd J; Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Singh M; Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Palafox MF; Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Wei A; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Elliott K; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Goodloe DH; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
    Dean SJ; Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
    Gooch C; Department of Pediatrics, Washington University School of Medicine in St. Louis, St. Louis, Missouri, USA.
    Murray BK; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, Virginia, USA.
    Swartz E; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, Virginia, USA.
    Schrier Vergano SA; Division of Medical Genetics and Metabolism, Children's Hospital of The King's Daughters, Norfolk, Virginia, USA.
    Towne MC; Ambry Genetics Corp, Aliso Viejo, California, USA.
    Nugent K; Department of Pediatrics, Baylor College of Medicine, San Antonio, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
    Roeder ER; Department of Pediatrics, Baylor College of Medicine, San Antonio, Texas, USA.; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
    Kresge C; Department of Pediatrics, Division of Clinical Genetics, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
    Pletcher BA; Department of Pediatrics, Division of Clinical Genetics, Rutgers New Jersey Medical School, Newark, New Jersey, USA.
    Grand K; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California, USA.
    Graham JM Jr; Department of Pediatrics, Cedars-Sinai Medical Center, Los Angeles, California, USA.
    Gates R; Department of Pediatrics, Division of Medical Genetics, Stanford University, Stanford, California, USA.
    Gomez-Ospina N; Department of Pediatrics, Division of Medical Genetics, Stanford University, Stanford, California, USA.
    Ramanathan S; Department of Pediatrics, Division of Medical Genetics, Loma Linda University Children's Hospital, Loma Linda, California, USA.
    Clark RD; Department of Pediatrics, Division of Medical Genetics, Loma Linda University Children's Hospital, Loma Linda, California, USA.
    Glaser K; Division of Genetics, Joe DiMaggio Children's Hospital, Hollywood, Florida, USA.
    Benke PJ; Division of Genetics, Joe DiMaggio Children's Hospital, Hollywood, Florida, USA.
    Cohen JS; Department of Neurology and Developmental Medicine, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Department of Neurology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
    Fatemi A; Department of Neurology and Developmental Medicine, Kennedy Krieger Institute, Baltimore, Maryland, USA.; Department of Neurology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
    Mu W; Department of Genetic Medicine, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
    Baranano KW; Department of Neurology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
    Madden JA; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.
    Gubbels CS; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    Yu TW; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    Agrawal PB; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.; The Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, Massachusetts, USA.; Division of Newborn Medicine, Department of Pediatrics, Boston Children's Hospital, Boston, Massachusetts, USA.
    Chambers MK; Division of Human Genetics, Warren Alpert Medical School of Brown University, Hasbro Children's Hospital/Rhode Island Hospital, Providence, Rhode Island, USA.
    Phornphutkul C; Division of Human Genetics, Warren Alpert Medical School of Brown University, Hasbro Children's Hospital/Rhode Island Hospital, Providence, Rhode Island, USA.
    Pugh JA; Division of Child Neurology, Department of Neurology, Albany Medical Center, Albany, New York, USA.
    Tauber KA; Division of Neonatology, Department of Pediatrics, Albany Medical Center, Bernard and Millie Duker Children's Hospital, Albany, New York, USA.
    Azova S; Division of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    Smith JR; Division of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    O'Donnell-Luria A; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    Medsker H; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    Srivastava S; Department of Neurology, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
    Krakow D; Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.; Department of Obstetrics and Gynecology, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Schweitzer DN; Division of Medical Genetics, Department of Pediatrics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Arboleda VA; Department of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.; Department of Pathology and Laboratory Medicine, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
    Pokaż więcej
    Źródło:
    Molecular genetics & genomic medicine [Mol Genet Genomic Med] 2021 Oct; Vol. 9 (10), pp. e1809. Date of Electronic Publication: 2021 Sep 14.
    Typ publikacji:
    Journal Article; Research Support, N.I.H., Extramural
    MeSH Terms:
    Genetic Association Studies*
    Genetic Predisposition to Disease*
    Mutation*
    Phenotype*
    Histone Acetyltransferases/*genetics
    Abnormalities, Multiple/diagnosis ; Abnormalities, Multiple/genetics ; Alleles ; Blepharophimosis/diagnosis ; Blepharophimosis/genetics ; Cohort Studies ; Congenital Hypothyroidism/diagnosis ; Congenital Hypothyroidism/genetics ; Craniofacial Abnormalities/diagnosis ; Craniofacial Abnormalities/genetics ; Facies ; Genetic Counseling ; Genetic Loci ; Genotype ; Heart Defects, Congenital/diagnosis ; Heart Defects, Congenital/genetics ; Humans ; Intellectual Disability/diagnosis ; Intellectual Disability/genetics ; Joint Instability/diagnosis ; Joint Instability/genetics ; Kidney/abnormalities ; Male ; Patella/abnormalities ; Psychomotor Disorders/diagnosis ; Psychomotor Disorders/genetics ; Scrotum/abnormalities ; Urogenital Abnormalities/diagnosis ; Urogenital Abnormalities/genetics
    SCR Disease Name:
    Genitopatellar Syndrome; Young Simpson syndrome
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknie Pełny tekstSzczegóły
    Tytuł:
    Prevention of postnatal growth restriction by the implementation of an evidence-based premature infant feeding bundle.
    Autorzy:
    Graziano PD; Nursing (Neonatology), Albany Medical Center, Albany, NY, USA.
    Tauber KA; Pediatrics (Neonatology), Children's Hospital at Albany Medical Center, Albany, NY, USA.
    Cummings J; Pediatrics (Neonatology), Children's Hospital at Albany Medical Center, Albany, NY, USA.
    Graffunder E; Epidemiology, Albany Medical Center, Albany, NY, USA.
    Horgan MJ; Pediatrics (Neonatology), Children's Hospital at Albany Medical Center, Albany, NY, USA.
    Pokaż więcej
    Źródło:
    Journal of perinatology : official journal of the California Perinatal Association [J Perinatol] 2015 Aug; Vol. 35 (8), pp. 642-9. Date of Electronic Publication: 2015 Apr 16.
    Typ publikacji:
    Journal Article
    MeSH Terms:
    Infant Nutritional Physiological Phenomena*
    Enteral Nutrition/*methods
    Enterocolitis, Necrotizing/*prevention & control
    Infant, Extremely Premature/*growth & development
    Infant, Very Low Birth Weight/*growth & development
    Evidence-Based Practice ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Milk, Human ; Prospective Studies ; Weight Gain
    Czasopismo naukowe
    Pełny tekst  Link otwiera się w nowym oknieSzczegóły
      Wyświetlanie 1-4 z 4

      Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies