UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 79

Sortiert nach

Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines

International journal of molecular sciences, 2024-04, Vol.25 (7), p.3586

2024

Link zum Volltext

Verfügbarkeit prüfen

Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias

Fetal and pediatric pathology, 2024-05, Vol.43 (3), p.257-265

2024

Link zum Volltext

Verfügbarkeit prüfen

Depression and Anxiety in Pediatric Patients with Beckwith-Wiedemann Syndrome: A Pilot Study

Children (Basel), 2024-03, Vol.11 (3), p.342

2024

Link zum Volltext

Verfügbarkeit prüfen

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Plastic and reconstructive surgery. Global open, 2024-03, Vol.12 (3), p.e5635

2024

Link zum Volltext

Verfügbarkeit prüfen

Beckwith–Wiedemann syndrome with juvenile fibrous nodules and lobular breast tumors: a case report and review of the literature

Surgical case reports, 2024-03, Vol.10 (1), p.69-69

2024

Link zum Volltext

Verfügbarkeit prüfen

Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

Archives of endocrinology and metabolism, 2024-02, Vol.68, p.e220395

2024

Link zum Volltext

Verfügbarkeit prüfen

A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome

International journal of surgery case reports, 2024-06, Vol.119, Article 109777

2024

Link zum Volltext

Verfügbarkeit prüfen

Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith–Wiedemann Syndrome

Annals of laboratory medicine, 2022-11, p.668-677

2022

Link zum Volltext

Verfügbarkeit prüfen

Tongue Reduction Surgery Improves Mandibular Prognathism in Beckwith-Wiedemann Syndrome Without Compromising Tongue Function

Clinical and experimental otorhinolaryngology, 2023-02, p.67-74

2023

Link zum Volltext

Verfügbarkeit prüfen

P369: Acute lymphocytic leukemia in a child with Beckwith Wiedemann syndrome: Coincidence or related to loss of CDKN1C function?

Genetics in Medicine Open, 2024, Vol.2, p.101263

2024

Link zum Volltext

Verfügbarkeit prüfen

Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome

Journal of pathology and translational medicine, 2019-03, p.129-135

2019

Link zum Volltext

Verfügbarkeit prüfen

Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome

Genes & genomics, 2013-04, p.141-147

2013

Link zum Volltext

Verfügbarkeit prüfen

Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature

Frontiers in pediatrics, 2024-03, Vol.12, p.1334544

2024

Link zum Volltext

Verfügbarkeit prüfen

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Plastic and reconstructive surgery. Global open, 2024, Vol.12 (3), p.e5635-e5635

2024

Link zum Volltext

Verfügbarkeit prüfen

Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum

Autopsy & case reports, 2024, Vol.14, p.e2024486

2024

Link zum Volltext

Verfügbarkeit prüfen

A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

Genes & development, 2024-03, Vol.38 (3-4), p.131

2024

Link zum Volltext

Verfügbarkeit prüfen

Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum

Autopsy & case reports, 2024, Vol.14, p.e2024486-e2024486

2024

Link zum Volltext

Verfügbarkeit prüfen

Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature

Frontiers in pediatrics, 2024, Vol.12, p.1334544-1334544

2024

Link zum Volltext

Verfügbarkeit prüfen

Approach to the Neonate with Hypoglycemia

The journal of clinical endocrinology and metabolism, 2024-04

2024

Link zum Volltext

Verfügbarkeit prüfen

Detection of 4p16.3 deletion and 11p15.5p15.4 gain in a boy by comparative genomic hybridization array: A case report

World journal of clinical cases, 2024-03, Vol.12 (8), p.1517-1522

Kaya, Işın

2024

Link zum Volltext

Verfügbarkeit prüfen

Huge mesenchymal hamartoma in a young adult: a case report

Journal of surgical case reports, 2024-04, Vol.2024 (4), p.rjae184

2024

Link zum Volltext

Verfügbarkeit prüfen

Simpson-Golabi-Behmel syndrome type 1 with normal birth parameters

BMJ case reports, 2024-03, Vol.17 (3)

2024

Link zum Volltext

Verfügbarkeit prüfen

Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors

Genes, 2024-02, Vol.15 (3), p.321

2024

Link zum Volltext

Verfügbarkeit prüfen

Further Delineation of Clinical Phenotype of IZMYND11/I Variants in Patients with Neurodevelopmental Dysmorphic Syndrome

Genes, 2024-02, Vol.15 (2)

2024

Link zum Volltext

Verfügbarkeit prüfen

Review of Opsoclonus-Myoclonus Ataxia Syndrome in Pediatric Patients

Children (Basel), 2024-03, Vol.11 (3), p.367

2024

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 79

Suche als RSS-Feed

Aktive Filter

KollektionWiley Online Library All Journals

Neu hinzugefügt... seit 90 Tagen

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(56)
Mit Volltextzugriff
(53)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(22)
... seit 7 Tagen
(11)

Menü

Weitere Dienste

Einstellungen

Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell Lines

Novel Autopsy Findings in Premature Infant With Beckwith-Wiedemann Syndrome Uniparental Disomy: Multifocal Developmental Dysplastic Chrondromatous Lesions and Cortical Neuronal Heterotopias

Depression and Anxiety in Pediatric Patients with Beckwith-Wiedemann Syndrome: A Pilot Study

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Beckwith–Wiedemann syndrome with juvenile fibrous nodules and lobular breast tumors: a case report and review of the literature

Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

A rare case of extremely low birth weight infant with Beckwith-Wiedemann syndrome

Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith–Wiedemann Syndrome

Tongue Reduction Surgery Improves Mandibular Prognathism in Beckwith-Wiedemann Syndrome Without Compromising Tongue Function

P369: Acute lymphocytic leukemia in a child with Beckwith Wiedemann syndrome: Coincidence or related to loss of CDKN1C function?

Adrenal Cortical Neoplasm with Uncertain Malignant Potential Arising in the Heterotopic Adrenal Cortex in the Liver of a Patient with Beckwith-Wiedemann Syndrome

Novel mutations of CDKN1C in Japanese patients with Beckwith-Wiedemann syndrome

Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature

Effective Collaboration in the Surgical Management of Macroglossia in Beckwith-Wiedemann Syndrome

Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum

A maternal-effect Padi6 variant causes nuclear and cytoplasmic abnormalities in oocytes, as well as failure of epigenetic reprogramming and zygotic genome activation in embryos

Trisomy 13 with unusual histological features typically described in Beckwith-Wiedemann Spectrum

Fetal Wilm's tumor detection preceding the development of isolated lateralized overgrowth of the limb: a case report and review of literature

Approach to the Neonate with Hypoglycemia

Detection of 4p16.3 deletion and 11p15.5p15.4 gain in a boy by comparative genomic hybridization array: A case report

Huge mesenchymal hamartoma in a young adult: a case report

Simpson-Golabi-Behmel syndrome type 1 with normal birth parameters

Understanding the Variability of 22q11.2 Deletion Syndrome: The Role of Epigenetic Factors

Further Delineation of Clinical Phenotype of IZMYND11/I Variants in Patients with Neurodevelopmental Dysmorphic Syndrome

Review of Opsoclonus-Myoclonus Ataxia Syndrome in Pediatric Patients

Aktive Filter

Suchergebnisse filtern