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...

A novel harbor seal whiskers optimization algorithm

Alexandria engineering journal, 2023-10, Vol.80, p.88-109

2023

Volltextzugriff (PDF)

Studies on some Economic Lepidopteran Pests of Date Palm Fruits and their Associated Parasitoid and Predatory Species in Siwa Oasis, Egypt

Egyptian journal of biological pest control, 2016-01, Vol.26 (3), p.497

2016

Volltextzugriff (PDF)

Untangling the tingle: Investigating the association between the Autonomous Sensory Meridian Response (ASMR), neuroticism, and trait & state anxiety

PloS one, 2022-02, Vol.17 (2), p.e0262668-e0262668

2022

Volltextzugriff (PDF)

A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasia

Journal of human genetics, 2022-11, Vol.67 (11), p.669-673

2022

Volltextzugriff (PDF)

Synthesis, characterization and DFT molecular modeling of doped poly (para-nitroaniline-co-para-toluidine) thin film for optoelectronic devices applications

Optical materials, 2020-01, Vol.99, p.109593, Article 109593

2020

Volltextzugriff (PDF)

Layered SnSe functionalized carbon composite as high-performance supercapacitor electrode

Materials research bulletin, 2023-12, Vol.168, p.112456, Article 112456

2023

Volltextzugriff (PDF)

Cytogenetic and clinical description of maternally inherited pure trisomy 4p

Middle East Journal of Medical Genetics, 2024-08

2024

Volltextzugriff (PDF)

Potential ameliorative role of Spirulina platensis in powdered or extract forms against cyclic heat stress in broiler chickens

Environmental science and pollution research international, 2022-06, Vol.29 (30), p.45578-45588

2022

Volltextzugriff (PDF)

Perovskite ceramics: the impact of lanthanum doping on the structural, radiation shielding and vibrational characteristics of lead titanate

Applied physics. A, Materials science & processing, 2024-05, Vol.130 (5), Article 348

2024

Volltextzugriff (PDF)

Polystyrene sulfonate coated activated graphene aerogel for boosting desalination performance using capacitive deionization

Separation and purification technology, 2022-10, Vol.299, p.121760, Article 121760

2022

Volltextzugriff (PDF)

Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation

Cytogenetic and genome research, 2020-04, Vol.160 (3), p.124-133

2020

Volltextzugriff (PDF)

Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features

Cytogenetic and genome research, 2019-01, Vol.159 (3), p.130-136

2019

Volltextzugriff (PDF)

A Possible Novel Protective Effect of Piceatannol against Isoproterenol (ISO)-Induced Histopathological, Histochemical, and Immunohistochemical Changes in Male Wistar Rats

Current issues in molecular biology, 2022-05, Vol.44 (6), p.2505-2528

2022

Volltextzugriff (PDF)

Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations

Prenatal diagnosis, 2020-04, Vol.40 (5), p.565-576

2020

Volltextzugriff (PDF)

Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion

Neuropediatrics, 2020-02, Vol.51 (1), p.76-82

2020

Volltextzugriff (PDF)

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

Molecular genetics & genomic medicine, 2021-11, Vol.9 (11), p.e1829-n/a

2021

Volltextzugriff (PDF)

Erratum: Clinical Variability of Pallister–Killian Syndrome in Two Egyptian Patients

Journal of pediatric genetics (Birmingham, Ala.), 2020-09, Vol.9 (3), p.e1-e1

2020

Volltextzugriff (PDF)

Response to letter from Okoye JO and Ngokere AA “Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?”

Prenatal diagnosis, 2020-12, Vol.40 (12), p.1618-1619

2020

Volltextzugriff (PDF)

Hydroxyapatite-based bio-ceramic of ternary nanocomposites containing cuprous oxide/graphene oxide for biomedical applications

Diamond and related materials, 2022-06, Vol.126, p.109121, Article 109121

2022

Volltextzugriff (PDF)

De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder

Pediatric dermatology, 2016-03, Vol.33 (2), p.e109-e113

2016

Volltextzugriff (PDF)

AB1059 Clinical and Electrophysiological Evaluation of The Effectiveness of Local Insulin Injection in Management of Idiopathic Carpal Tunnel Syndrome (Prospective Study)

Annals of the rheumatic diseases, 2016-06, Vol.75 (Suppl 2), p.1264-1264

2016

Volltextzugriff (PDF)

A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder

American journal of medical genetics. Part A, 2011-11, Vol.155 (11), p.2885-2896

2011

Volltextzugriff (PDF)

Vitamin D Levels in Non-alcoholic Fatty Liver Disease in Type II Diabetic and Non-Diabetic Patients

Bioactive compounds in health and disease, 2023-09, Vol.6 (9), p.202

2023

Volltextzugriff (PDF)

Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia

American journal of medical genetics. Part A, 2019-06, Vol.179 (6), p.1053-1057

2019

Volltextzugriff (PDF)

Clinical and cytogenetic assessment of a cohort of Egyptian patients with Neurofibromatosis 1

Gene reports, 2020-03, Vol.18, p.100573, Article 100573

2020

Volltextzugriff (PDF)

1 – 25 von 48

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(39)

Publikationsform

Sprache

Englisch
(48)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

A novel harbor seal whiskers optimization algorithm

Studies on some Economic Lepidopteran Pests of Date Palm Fruits and their Associated Parasitoid and Predatory Species in Siwa Oasis, Egypt

Untangling the tingle: Investigating the association between the Autonomous Sensory Meridian Response (ASMR), neuroticism, and trait & state anxiety

A homozygous loss-of-function variant in BICD2 is associated with lissencephaly and cerebellar hypoplasia

Synthesis, characterization and DFT molecular modeling of doped poly (para-nitroaniline-co-para-toluidine) thin film for optoelectronic devices applications

Layered SnSe functionalized carbon composite as high-performance supercapacitor electrode

Cytogenetic and clinical description of maternally inherited pure trisomy 4p

Potential ameliorative role of Spirulina platensis in powdered or extract forms against cyclic heat stress in broiler chickens

Perovskite ceramics: the impact of lanthanum doping on the structural, radiation shielding and vibrational characteristics of lead titanate

Polystyrene sulfonate coated activated graphene aerogel for boosting desalination performance using capacitive deionization

Two Abnormal Cell Lines of Trisomy 14 and t(X;14) with Skewed X-Inactivation

Bilateral Calcification of Basal Ganglia in a Patient with Duplication of Both 11q13.1q22.1 and 4q35.2 with New Phenotypic Features

A Possible Novel Protective Effect of Piceatannol against Isoproterenol (ISO)-Induced Histopathological, Histochemical, and Immunohistochemical Changes in Male Wistar Rats

Prenatal ultrasound findings of holoprosencephaly spectrum: Unusual associations

Further Insights into Developmental Brain Malformations and Leukoencephalopathy Associated with 6p25.3 Deletion

Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly

Erratum: Clinical Variability of Pallister–Killian Syndrome in Two Egyptian Patients

Response to letter from Okoye JO and Ngokere AA “Are the prevalence of Trisomy 13 and the incidence of severe holoprosencephaly increasing in Africa?”

Hydroxyapatite-based bio-ceramic of ternary nanocomposites containing cuprous oxide/graphene oxide for biomedical applications

De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder

AB1059 Clinical and Electrophysiological Evaluation of The Effectiveness of Local Insulin Injection in Management of Idiopathic Carpal Tunnel Syndrome (Prospective Study)

A homozygous mutation in RNU4ATAC as a cause of microcephalic osteodysplastic primordial dwarfism type I (MOPD I) with associated pigmentary disorder

Vitamin D Levels in Non-alcoholic Fatty Liver Disease in Type II Diabetic and Non-Diabetic Patients

Biallelic novel missense HHAT variant causes syndromic microcephaly and cerebellar‐vermis hypoplasia

Clinical and cytogenetic assessment of a cohort of Egyptian patients with Neurofibromatosis 1

Suchergebnisse filtern