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...

Impact of heat shock protein and tumour necrosis factor on klinefelter syndrome

New Zealand journal of medical laboratory science, 2023-07, Vol.77 (2), p.71-74

2023

Volltextzugriff (PDF)

Chemerin: An exploitable biomarker for familial Mediterranean fever in Egyptian patients

New Zealand journal of medical laboratory science, 2023-11, Vol.77 (3), p.114-118

2023

Volltextzugriff (PDF)

Serum levels of chemokines MCP-1, GRO-alpha and E-selectin correlates with familial Mediterranean fever

New Zealand journal of medical laboratory science, 2021-04, Vol.75 (1), p.21-25

2021

Volltextzugriff (PDF)

Brain derived neurotrophic factor, oxidative stress status and vitamin D levels in patients with autism spectrum disorder

New Zealand journal of medical laboratory science, 2022-03, Vol.76 (1), p.10-13

2022

Volltextzugriff (PDF)

Effect of obesity on serum IL-10 concentrations and messenger RNA expression in women with metabolic syndrome

New Zealand journal of medical laboratory science, 2022-07, Vol.76 (2), p.69-73

2022

Volltextzugriff (PDF)

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

Brain (London, England : 1878), 2020-08, Vol.143 (8), p.2388-2397

2020

Volltextzugriff (PDF)

Emanuel syndrome due to unusual pattern

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.21, Article 21

2024

Volltextzugriff (PDF)

Correction: Emanuel syndrome due to unusual pattern

Egyptian Journal of Medical Human Genetics, 2024-12, Vol.25 (1), p.75, Article 75

2024

Volltextzugriff (PDF)

Inflammatory and endothelial dysfunction indices among Egyptian females with obesity classes I-III

Bioscience reports, 2020-09, Vol.40 (9)

2020

Volltextzugriff (PDF)

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families

Genes, 2023-04, Vol.14 (4), p.900

2023

Volltextzugriff (PDF)

New diagnostic biomarkers for celiac disease in Egyptian children: Cyclophilin a and netrin-1

New Zealand journal of medical laboratory science, 2021-11, Vol.75 (3), p.189-191

2021

Volltextzugriff (PDF)

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

American journal of medical genetics. Part A, 2020-06, Vol.182 (6), p.1407-1420

2020

Volltextzugriff (PDF)

Evaluation of adropin, fibroblast growth factor-1 (FGF-1), and Toll-like receptor-1 (TLR1) biomarkers in patients with inflammatory bowel disease: gene expression of TNF-α as a marker of disease severity

The Egyptian journal of medical human genetics, 2024-06, Vol.25 (1), p.63

2024

Volltextzugriff (PDF)

Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease

Genes, 2021-09, Vol.12 (10), p.1552

2021

Volltextzugriff (PDF)

Evaluation of DNA damage profile in obese women and its association to risk of metabolic syndrome, polycystic ovary syndrome and recurrent preeclampsia

Genes & diseases, 2018-12, Vol.5 (4), p.367-373

2018

Volltextzugriff (PDF)

Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene

Egyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.28, Article 28

2022

Volltextzugriff (PDF)

Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex

Journal of Genetic Engineering and Biotechnology, 2022-02, Vol.20 (1), p.31, Article 31

2022

Volltextzugriff (PDF)

IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children

Journal of Genetic Engineering and Biotechnology, 2021-07, Vol.19 (1), p.109, Article 109

2021

Volltextzugriff (PDF)

Coenzyme Q10 and pro-inflammatory markers in children with Down syndrome: clinical and biochemical aspects

Jornal de pediatria, 2017-01, Vol.93 (1), p.100-104

2017

Volltextzugriff (PDF)

Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature

Egyptian Journal of Medical Human Genetics, 2020-09, Vol.21 (1), p.47, Article 47

2020

Volltextzugriff (PDF)

Altered expression of miR-17 and miR-148b in pediatric familial mediterranean fever patients

Clinical rheumatology, 2024-08, Vol.43 (8), p.2661-2667

2024

Volltextzugriff (PDF)

Growth curves of Egyptian patients with Turner syndrome

American journal of medical genetics. Part A, 2012-11, Vol.158A (11), p.2687-2691

2012

Volltextzugriff (PDF)

The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome

Journal of Pediatric Endocrinology and Metabolism, 2023-02, Vol.36 (2), p.147

2023

Volltextzugriff (PDF)

The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women

Molecular biology reports, 2021-05, Vol.48 (5), p.4413-4420

2021

Volltextzugriff (PDF)

Sialic acid and anti-ganglioside M1 antibodies are invaluable biomarkers correlated with the severity of autism spectrum disorder

Brain & development (Tokyo. 1979), 2023-04, Vol.45 (4), p.212-219

2023

Volltextzugriff (PDF)

1 – 25 von 120

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(91)
Mit Volltextzugriff
(89)

Publikationsform

Artikel
(115)
Berichte
(5)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(4)

Menü

Weitere Dienste

Einstellungen

Impact of heat shock protein and tumour necrosis factor on klinefelter syndrome

Chemerin: An exploitable biomarker for familial Mediterranean fever in Egyptian patients

Serum levels of chemokines MCP-1, GRO-alpha and E-selectin correlates with familial Mediterranean fever

Brain derived neurotrophic factor, oxidative stress status and vitamin D levels in patients with autism spectrum disorder

Effect of obesity on serum IL-10 concentrations and messenger RNA expression in women with metabolic syndrome

Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants

Emanuel syndrome due to unusual pattern

Correction: Emanuel syndrome due to unusual pattern

Inflammatory and endothelial dysfunction indices among Egyptian females with obesity classes I-III

Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families

New diagnostic biomarkers for celiac disease in Egyptian children: Cyclophilin a and netrin-1

Microcephalic osteodysplastic primordial dwarfism type II: Additional nine patients with implications on phenotype and genotype correlation

Evaluation of adropin, fibroblast growth factor-1 (FGF-1), and Toll-like receptor-1 (TLR1) biomarkers in patients with inflammatory bowel disease: gene expression of TNF-α as a marker of disease severity

Genetic and Molecular Evaluation: Reporting Three Novel Mutations and Creating Awareness of Pycnodysostosis Disease

Evaluation of DNA damage profile in obese women and its association to risk of metabolic syndrome, polycystic ovary syndrome and recurrent preeclampsia

Broadening the clinical spectrum of ALGS: an Egyptian cohort with five novel mutations in JAG1 gene

Dynamic disequilibrium-based pathogenicity model in mutated pyrin’s B30.2 domain—Casp1/p20 complex

IGF1R, IGFALS, and IGFBP3 gene copy number variations in a group of non-syndromic Egyptian short children

Coenzyme Q10 and pro-inflammatory markers in children with Down syndrome: clinical and biochemical aspects

Screening of the SHOX/PAR1 region using MLPA and miRNA expression profiling in a group of Egyptian children with non-syndromic short stature

Altered expression of miR-17 and miR-148b in pediatric familial mediterranean fever patients

Growth curves of Egyptian patients with Turner syndrome

The role of the deficiency of vitamin B12 and folic acid on homocysteinemia in children with Turner syndrome

The correlation of estrogen receptor 1 and progesterone receptor genes polymorphisms with recurrent pregnancy loss in a cohort of Egyptian women

Sialic acid and anti-ganglioside M1 antibodies are invaluable biomarkers correlated with the severity of autism spectrum disorder

Suchergebnisse filtern