UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

Oral health status of Egyptian children with lysosomal storage diseases: An evaluation of dental indices, salivary cytokines level, and bacterial bioburden

International journal of paediatric dentistry, 2024-05

2024

Volltextzugriff (PDF)

Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Annals of Pediatric Endocrinology & Metabolism, 2022, 27(3), , pp.214-222

2022

Volltextzugriff (PDF)

Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion

Egyptian Journal of Medical Human Genetics, 2024-07, Vol.25 (1), p.88, Article 88

2024

Volltextzugriff (PDF)

Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome

American journal of human genetics, 2011-01, Vol.88 (1), p.92-98

2011

Volltextzugriff (PDF)

Health Related Quality of Life of Under Five Children with Down Syndrome and Sociodemographic Correlates

Journal of High Institute of Public Health, 2023-08, Vol.53 (1), p.1-9

2023

Volltextzugriff (PDF)

Results From a 12-Month Open-Label Phase 1/2 Study of Velaglucerase Alfa in Children and Adolescents With Type 3 Gaucher Disease

Journal of inborn errors of metabolism and screening, 2018, Vol.6, p.232640981876556

2018

Volltextzugriff (PDF)

An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

European journal of human genetics : EJHG, 2022-09, Vol.30 (9), p.1029-1035

2022

Volltextzugriff (PDF)

Immunoglobulin-G subclass pattern among children with mucopolysaccharidosis attending the genetic clinic of Alexandria University Children’s Hospital

Alexandria Journal of Pediatrics, 2022-01, Vol.35 (1), p.1-7

2022

Volltextzugriff (PDF)

Hyperimmunoglobulinemia and IgG Subclass Abnormalities in Children With Gaucher Disease

Journal of pediatric hematology/oncology, 2019-10, Vol.41 (7), p.e416-e420

2019

Volltextzugriff (PDF)

Echocardiographic findings in infants of diabetic mothers and their relation to maternal glycemic control

Alexandria Journal of Pediatrics, 2023-01, Vol.36 (1), p.1-14

2023

Volltextzugriff (PDF)

Prevalence of celiac disease among children with Down syndrome attending the genetics clinic at Alexandria University Children Hospital

Alexandria Journal of Pediatrics, 2020-01, Vol.33 (1), p.1

2020

Volltextzugriff (PDF)

Assessment of cluster of differentiation 4 and 8 among children with trisomy 21

Alexandria Journal of Pediatrics, 2021-01, Vol.34 (1), p.29-39

2021

Volltextzugriff (PDF)

Mutations in ALDH1A3 Represent a Frequent Cause of Microphthalmia/Anophthalmia in Consanguineous Families

Human mutation, 2014-08, Vol.35 (8), p.949-953

2014

Volltextzugriff (PDF)

Velaglucerase alfa enzyme replacement therapy in children and adolescents with type 3 Gaucher disease: Results of a 12-month multicenter, open-label phase 1/2 study

Molecular genetics and metabolism, 2016-02, Vol.117 (2), p.S111-S111

2016

Volltextzugriff (PDF)

Registry of ocular anomalies among patients with genetic disorders in Alexandria and nearby governorates

Alexandria Journal of Pediatrics, 2019-01, Vol.32 (1), p.55

2019

Volltextzugriff (PDF)

Clinical characteristics of type III Gaucher disease in children and adolescents enrolled in a trial of velaglucerase alfa

Molecular genetics and metabolism, 2015-02, Vol.114 (2), p.S21-S21

2015

Volltextzugriff (PDF)

RAX and anophthalmia in humans: evidence of brain anomalies

Molecular vision, 2012-06, Vol.18, p.1449-1456

2012

Volltextzugriff (PDF)

FREQUENCY OF MAJOR CONGENITAL ANOMALIES IN NEONATES ADMITTED TO INTENSIVE CARE UNIT AT ALEXANDRIA UNIVERSITY CHILDREN'S HOSPITAL

ALEXMED ePosters, 2022-07, Vol.4 (3), p.22-23

2022

Volltextzugriff (PDF)

Quality of life assessment in patients with duchenne muscular dystrophy

International journal of health sciences, 2022-06, p.15040-15049

2022

Volltextzugriff (PDF)

DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE

ALEXMED ePosters, 2022-06, Vol.4 (2), p.10-11

2022

Volltextzugriff (PDF)

Molecular basis of beta-thalassemia in Alexandria

The Egyptian journal of immunology, 2005, Vol.12 (1), p.15

2005

Volltextzugriff (PDF)

Markers of apoptosis and proliferation related gene products as predictors of treatment outcome in childhood acute lymphoblastic leukemia

Hematology (Luxembourg), 2007-06, Vol.12 (3), p.209-218

2007

Volltextzugriff (PDF)

Late-onset systemic lupus erythematosus: characteristics and outcome in comparison to juvenile- and adult-onset patients—a multicenter retrospective cohort

Clinical rheumatology, 2020-02, Vol.39 (2), p.435-442

2020

Volltextzugriff (PDF)

Comparative Taxonomic Study of Launaea Cass. (Asteraceae, Cichorioideae) in Egypt

Taxonomy (Basel, Switzerland), 2021-09, Vol.1 (3), p.192-209

2021

Volltextzugriff (PDF)

A comparative study between the disease characteristics in adult-onset and childhood-onset systemic lupus erythematosus in Egyptian patients attending a large university hospital

Lupus, 2021-02, Vol.30 (2), p.211-218

2021

Volltextzugriff (PDF)

1 – 25 von 41

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(34)
Mit Volltextzugriff
(33)

Publikationsform

Artikel
(40)
Berichte
(1)

Sprache

Englisch
(41)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Oral health status of Egyptian children with lysosomal storage diseases: An evaluation of dental indices, salivary cytokines level, and bacterial bioburden

Clinical and molecular characteristics of infantile-onset diabetes mellitus in Egypt

Diagnosis and management of patients with Gaucher disease: an Egyptian expert opinion

Mutations in the SPARC-Related Modular Calcium-Binding Protein 1 Gene, SMOC1, Cause Waardenburg Anophthalmia Syndrome

Health Related Quality of Life of Under Five Children with Down Syndrome and Sociodemographic Correlates

Results From a 12-Month Open-Label Phase 1/2 Study of Velaglucerase Alfa in Children and Adolescents With Type 3 Gaucher Disease

An integrated multiomic approach as an excellent tool for the diagnosis of metabolic diseases: our first 3720 patients

Immunoglobulin-G subclass pattern among children with mucopolysaccharidosis attending the genetic clinic of Alexandria University Children’s Hospital

Hyperimmunoglobulinemia and IgG Subclass Abnormalities in Children With Gaucher Disease

Echocardiographic findings in infants of diabetic mothers and their relation to maternal glycemic control

Prevalence of celiac disease among children with Down syndrome attending the genetics clinic at Alexandria University Children Hospital

Assessment of cluster of differentiation 4 and 8 among children with trisomy 21

Mutations in ALDH1A3 Represent a Frequent Cause of Microphthalmia/Anophthalmia in Consanguineous Families

Velaglucerase alfa enzyme replacement therapy in children and adolescents with type 3 Gaucher disease: Results of a 12-month multicenter, open-label phase 1/2 study

Registry of ocular anomalies among patients with genetic disorders in Alexandria and nearby governorates

Clinical characteristics of type III Gaucher disease in children and adolescents enrolled in a trial of velaglucerase alfa

RAX and anophthalmia in humans: evidence of brain anomalies

FREQUENCY OF MAJOR CONGENITAL ANOMALIES IN NEONATES ADMITTED TO INTENSIVE CARE UNIT AT ALEXANDRIA UNIVERSITY CHILDREN'S HOSPITAL

Quality of life assessment in patients with duchenne muscular dystrophy

DETECTION OF MICRODELETION IN CHROMOSOME 7q11.23 BY FLUORESCENT IN SITU HYBRIDIZATION TECHNIQUE AMONG AN EGYPTIAN COHORT SUSPECTED TO HAVE WILLIAMS SYNDROMRE

Molecular basis of beta-thalassemia in Alexandria

Markers of apoptosis and proliferation related gene products as predictors of treatment outcome in childhood acute lymphoblastic leukemia

Late-onset systemic lupus erythematosus: characteristics and outcome in comparison to juvenile- and adult-onset patients—a multicenter retrospective cohort

Comparative Taxonomic Study of Launaea Cass. (Asteraceae, Cichorioideae) in Egypt

A comparative study between the disease characteristics in adult-onset and childhood-onset systemic lupus erythematosus in Egyptian patients attending a large university hospital

Suchergebnisse filtern