UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 84

Sortiert nach

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis

Genetics in medicine, 2018-07, Vol.20 (7), p.745-753

2018

Volltextzugriff (PDF)

Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype

Human genetics, 2019-12, Vol.138 (11-12), p.1301-1311

2019

Volltextzugriff (PDF)

Workload Measurement in Subspecialty Placental Pathology in Canada

Pediatric and developmental pathology, 2022-11, Vol.25 (6), p.604-610

2022

Volltextzugriff (PDF)

Presence of autoantibodies against tubular and uveal cells in a patient with tubulointerstitial nephritis and uveitis (TINU) syndrome

Nephrology, dialysis, transplantation, 2008-04, Vol.23 (4), p.1452-1455

2008

Volltextzugriff (PDF)

Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study

American journal of clinical pathology, 2014-07, Vol.142 (1), p.104-110

2014

Volltextzugriff (PDF)

Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with a de Novo Heterozygous Mutation in the TITF1/NKX2.1 Gene

The journal of clinical endocrinology and metabolism, 2009-01, Vol.94 (1), p.197-203

2009

Volltextzugriff (PDF)

Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis

Obstetrical & gynecological survey, 2018-12, Vol.73 (12), p.677-679

2018

Volltextzugriff (PDF)

Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping

Clinical case reports, 2021-03, Vol.9 (3), p.1101-1103

2021

Volltextzugriff (PDF)

Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13

Journal of pediatric intensive care, 2020-03, Vol.9 (1), p.054-059

2020

Volltextzugriff (PDF)

Pediatric Anogenital Warts: A 7-Year Review of Children Referred to a Tertiary-Care Hospital in Montreal, Canada

Pediatric dermatology, 2006-05, Vol.23 (3), p.199-207

2006

Volltextzugriff (PDF)

AKT pathway in neuroblastoma and its therapeutic implication

Expert review of anticancer therapy, 2008-05, Vol.8 (5), p.757-769

2008

Volltextzugriff (PDF)

The Adipose Tissue Phenotype of Hormone-Sensitive Lipase Deficiency in Mice

Obesity (Silver Spring, Md.), 2001-02, Vol.9 (2), p.119-128

2001

Volltextzugriff (PDF)

Intrauterine growth restriction in rats is associated with hypertension and renal dysfunction in adulthood

American journal of physiology: endocrinology and metabolism, 2002-07, Vol.283 (1), p.E124-E131

2002

Volltextzugriff (PDF)

Sudden death in growth hormone–treated children with Prader-Willi syndrome

The Journal of pediatrics, 2004-01, Vol.144 (1), p.129-131

2004

Volltextzugriff (PDF)

High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastoma

Histopathology, 2010-04, Vol.56 (5), p.607-616

2010

Volltextzugriff (PDF)

Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities With Normal Karyotype

Journal of obstetrics and gynaecology Canada, 2011-10, Vol.33 (10), p.1047-1057

2011

Volltextzugriff (PDF)

Cardiac pathology in sudden unexpected infant death

The Journal of pediatrics, 2002-09, Vol.141 (3), p.336-342

2002

Volltextzugriff (PDF)

A B-cell lymphoma–associated chromosomal translocation in a progressive transformation of germinal center

Human pathology, 2008-02, Vol.39 (2), p.292-297

2008

Volltextzugriff (PDF)

Caudal dysgenesis, sirenomelia, and situs inversus totalis: A primitive defect in blastogenesis

American journal of medical genetics. Part A, 2008-06, Vol.146A (11), p.1470-1476

2008

Volltextzugriff (PDF)

Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies

The Journal of pediatrics, 2000-10, Vol.137 (4), p.585-587

2000

Volltextzugriff (PDF)

Unilobar congenital pulmonary lymphangiectasis mimicking congenital lobar emphysema: an underestimated presentation?

Journal of pediatric surgery, 2004-05, Vol.39 (5), p.677-680

2004

Volltextzugriff (PDF)

Intrahepatic Biliary Cysts Presenting before Hepatic Portoenterostomy in Biliary Atresia

Journal of pediatric gastroenterology and nutrition, 2006-04, Vol.42 (4), p.440-442

2006

Volltextzugriff (PDF)

Basal cells of second trimester fetal breasts: immunohistochemical study of myoepithelial precursors

Pediatric and developmental pathology, 2003-09, Vol.6 (5), p.398-413

2003

Volltextzugriff (PDF)

Accessory Liver Lobe with Mesothelial Inclusion Cysts in an Omphalocele: A New Malformative Association

Pediatric and developmental pathology, 2007-05, Vol.10 (3), p.224-228

2007

Volltextzugriff (PDF)

Cryptic recurrent ACIN1‐NUTM1 fusions in non‐KMT2A‐rearranged infant acute lymphoblastic leukemia

Genes chromosomes & cancer, 2020-02, Vol.59 (2), p.125-130

2020

Volltextzugriff (PDF)

1 – 25 von 84

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(81)
Mit Volltextzugriff
(82)

Publikationsform

Artikel
(81)
Berichte
(3)

Sprache

Erscheinungsjahr

n.n

Thema

Life Sciences & Biomedicine
(53)
Science & Technology
(53)
Humans
(47)
Female
(31)
Male
(25)
Biological And Medical Sciences
(24)
Medical Sciences
(22)
Pediatrics
(20)
Pathology
(18)
Child
(13)
Adult
(12)
Infant
(10)
Child, Preschool
(9)
Infant, Newborn
(8)
Pregnancy
(8)
Immunohistochemistry
(7)
Adolescent
(6)
Animals
(6)
Biopsy
(6)
Fundamental And Applied Biological Sciences. Psychology
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis

Association of rare non-coding SNVs in the lung-specific FOXF1 enhancer with a mitigation of the lethal ACDMPV phenotype

Workload Measurement in Subspecialty Placental Pathology in Canada

Presence of autoantibodies against tubular and uveal cells in a patient with tubulointerstitial nephritis and uveitis (TINU) syndrome

Assessment of correlation between p16INK4a staining, specific subtype of human papillomavirus, and progression of LSIL/CIN1 lesions: first comparative study

Lethal Respiratory Failure and Mild Primary Hypothyroidism in a Term Girl with a de Novo Heterozygous Mutation in the TITF1/NKX2.1 Gene

Genomic Study of Severe Fetal Anomalies and Discovery of GREB1L Mutations in Renal Agenesis

Prenatal presentation of glutaric aciduria type II: A case report with radiologic, clinical, biochemical, molecular, and pathological phenotyping

Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13

Pediatric Anogenital Warts: A 7-Year Review of Children Referred to a Tertiary-Care Hospital in Montreal, Canada

AKT pathway in neuroblastoma and its therapeutic implication

The Adipose Tissue Phenotype of Hormone-Sensitive Lipase Deficiency in Mice

Intrauterine growth restriction in rats is associated with hypertension and renal dysfunction in adulthood

Sudden death in growth hormone–treated children with Prader-Willi syndrome

High level of apoptosis and low AKT activation in mass screening as opposed to standard neuroblastoma

Fetal and Perinatal Autopsy in Prenatally Diagnosed Fetal Abnormalities With Normal Karyotype

Cardiac pathology in sudden unexpected infant death

A B-cell lymphoma–associated chromosomal translocation in a progressive transformation of germinal center

Caudal dysgenesis, sirenomelia, and situs inversus totalis: A primitive defect in blastogenesis

Hyperfunctioning malignant thyroid nodule in an 11-year-old girl: Pathologic and molecular studies

Unilobar congenital pulmonary lymphangiectasis mimicking congenital lobar emphysema: an underestimated presentation?

Intrahepatic Biliary Cysts Presenting before Hepatic Portoenterostomy in Biliary Atresia

Basal cells of second trimester fetal breasts: immunohistochemical study of myoepithelial precursors

Accessory Liver Lobe with Mesothelial Inclusion Cysts in an Omphalocele: A New Malformative Association

Cryptic recurrent ACIN1‐NUTM1 fusions in non‐KMT2A‐rearranged infant acute lymphoblastic leukemia

Suchergebnisse filtern