UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 26

Sortiert nach

Genetics of Azoospermia

International journal of molecular sciences, 2021-03, Vol.22 (6), p.3264

2021

Link zum Volltext

Verfügbarkeit prüfen

Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients’ and Offspring Health

Journal of clinical medicine, 2021-09, Vol.10 (17), p.4009

2021

Link zum Volltext

Verfügbarkeit prüfen

Testing for genetic contributions to infertility: potential clinical impact

Expert review of molecular diagnostics, 2018-04, Vol.18 (4), p.331-346

2018

Link zum Volltext

Verfügbarkeit prüfen

Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men

Genetics in medicine, 2020-12, Vol.22 (12), p.1956-1966

2020

Link zum Volltext

Verfügbarkeit prüfen

gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study

European journal of human genetics : EJHG, 2019-10, Vol.27 (10), p.1578-1588

2019

Link zum Volltext

Verfügbarkeit prüfen

Hypogonadism and sexual function in men affected by adrenocortical carcinoma under mitotane therapy

Frontiers in endocrinology (Lausanne), 2024-01, Vol.14, p.1320722-1320722

2024

Link zum Volltext

Verfügbarkeit prüfen

Age-Dependent De Novo Mutations During Spermatogenesis and Their Consequences

Genetic Damage in Human Spermatozoa, 2019-01, p.29-46

2019

Link zum Volltext

Verfügbarkeit prüfen

Severe sperm DNA fragmentation may persist for up to 3 years after cytotoxic therapy in patients affected by Hodgkin lymphoma and non-Hodgkin lymphoma

Human reproduction (Oxford), 2024-03, Vol.39 (3), p.496-503

2024

Link zum Volltext

Verfügbarkeit prüfen

FSCN1 as a new druggable target in adrenocortical carcinoma

International journal of cancer, 2023-07, Vol.153 (1), p.210-223

2023

Link zum Volltext

Verfügbarkeit prüfen

Long-term effect of cytotoxic treatments on sperm DNA fragmentation in patients affected by testicular germ cell tumor

Andrology (Oxford), 2023-11, Vol.11 (8), p.1653-1661

2023

Link zum Volltext

Verfügbarkeit prüfen

Genetics of Male Infertility

Encyclopedia of Endocrine Diseases, Second Edition, 2019, p.821-830

Second Edition, 2019

Link zum Volltext

Verfügbarkeit prüfen

Quality of life in Italian patients with Multiple endocrine neoplasia type 1 (MEN 1): results of an extensive survey

Orphanet journal of rare diseases, 2021-01, Vol.16 (1), p.16-16, Article 16

2021

Link zum Volltext

Verfügbarkeit prüfen

Secretin Stimulation Test and Early Diagnosis of Gastrinoma in MEN1 Syndrome: Survey on the MEN1 Florentine Database

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.e2110-e2123

2022

Link zum Volltext

Verfügbarkeit prüfen

Bone phenotypes in multiple endocrine neoplasia type 1: survey on the MEN1 Florentine database

Endocrine Connections, 2022-05, Vol.11 (5), p.1-12

2022

Link zum Volltext

Verfügbarkeit prüfen

Bone and Mineral Metabolism Phenotypes in MEN1-Related and Sporadic Primary Hyperparathyroidism, before and after Parathyroidectomy

Cells (Basel, Switzerland), 2021-07, Vol.10 (8), p.1895

2021

Link zum Volltext

Verfügbarkeit prüfen

ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of Hypophosphatasia

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.e2087-e2094

2022

Link zum Volltext

Verfügbarkeit prüfen

The LARO-MEN1 study: a longitudinal clinical experience with octreotide Long-Acting Release in patients with Multiple Endocrine Neoplasia type 1 Syndrome

Clinical cases in mineral and bone metabolism, 2017-05, Vol.14 (2), p.123-130

2017

Link zum Volltext

Verfügbarkeit prüfen

Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1)

Endocrine, 2016-06, Vol.52 (3), p.495-506

2016

Link zum Volltext

Verfügbarkeit prüfen

Two Novel Mutations at Exon 8 of the Sequestosome 1 (SQSTM1) Gene in an Italian Series of Patients Affected by Paget's Disease of Bone (PDB)

Journal of bone and mineral research, 2004-06, Vol.19 (6), p.1013-1017

2004

Link zum Volltext

Verfügbarkeit prüfen

Azidothymidine Induces Apoptosis and Inhibits Cell Growth and Telomerase Activity of Human Parathyroid Cancer Cells in Culture

Journal of bone and mineral research, 2005-03, Vol.20 (3), p.410-418

2005

Link zum Volltext

Verfügbarkeit prüfen

Social Media Influence on the Intellectual Capital Growth of Listed Companies

European Conference on Intangibles and Intellectual Capital, 2019, p.262-XIV

2019

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 26

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(24)
Mit Volltextzugriff
(23)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Genetics of Azoospermia

Genetic Factors of Non-Obstructive Azoospermia: Consequences on Patients’ and Offspring Health

Testing for genetic contributions to infertility: potential clinical impact

Genetic dissection of spermatogenic arrest through exome analysis: clinical implications for the management of azoospermic men

gr/gr deletion predisposes to testicular germ cell tumour independently from altered spermatogenesis: results from the largest European study

Hypogonadism and sexual function in men affected by adrenocortical carcinoma under mitotane therapy

Age-Dependent De Novo Mutations During Spermatogenesis and Their Consequences

Severe sperm DNA fragmentation may persist for up to 3 years after cytotoxic therapy in patients affected by Hodgkin lymphoma and non-Hodgkin lymphoma

FSCN1 as a new druggable target in adrenocortical carcinoma

Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure

Long-term effect of cytotoxic treatments on sperm DNA fragmentation in patients affected by testicular germ cell tumor

Genetics of Male Infertility

Quality of life in Italian patients with Multiple endocrine neoplasia type 1 (MEN 1): results of an extensive survey

Secretin Stimulation Test and Early Diagnosis of Gastrinoma in MEN1 Syndrome: Survey on the MEN1 Florentine Database

Bone phenotypes in multiple endocrine neoplasia type 1: survey on the MEN1 Florentine database

Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient database

Bone and Mineral Metabolism Phenotypes in MEN1-Related and Sporadic Primary Hyperparathyroidism, before and after Parathyroidectomy

ALPL Genotypes in Patients With Atypical Femur Fractures or Other Biochemical and Clinical Signs of Hypophosphatasia

The LARO-MEN1 study: a longitudinal clinical experience with octreotide Long-Acting Release in patients with Multiple Endocrine Neoplasia type 1 Syndrome

Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1)

Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database

Two Novel Mutations at Exon 8 of the Sequestosome 1 (SQSTM1) Gene in an Italian Series of Patients Affected by Paget's Disease of Bone (PDB)

Correction to: Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database

Azidothymidine Induces Apoptosis and Inhibits Cell Growth and Telomerase Activity of Human Parathyroid Cancer Cells in Culture

Social Media Influence on the Intellectual Capital Growth of Listed Companies

Suchergebnisse filtern