UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 29

Sortiert nach

Efficacy and safety of burosumab compared with conventional therapy in patients with X-linked hypophosphatemia: A systematic review

Archives of Endocrinology and Metabolism, 2024-05, Vol.68, p.e230242

2024

Volltextzugriff (PDF)

177Lu-DOTATATE therapy in metastatic/inoperable pheochromocytoma-paraganglioma

Endocrine Connections, 2020-09, Vol.9 (9), p.864-873

2020

Volltextzugriff (PDF)

Predictors of Chronic LH-Testosterone Axis Suppression in Male Macroprolactinomas With Normoprolactinemia on Cabergoline

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-e4557

2020

Volltextzugriff (PDF)

Metastatic cluster 2-related pheochromocytoma/paraganglioma: a single-center experience and systematic review

Endocrine Connections, 2021-11, Vol.10 (11), p.1463-1476

2021

Volltextzugriff (PDF)

Vitamin D deficiency or resistance and hypophosphatemia

Best Practice & Research Clinical Endocrinology & Metabolism, 2024-03, Vol.38 (2), p.101876, Article 101876

2024

Volltextzugriff (PDF)

Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?

Neuroendocrinology, 2024, Vol.114 (1), p.42

2024

Volltextzugriff (PDF)

Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review

Calcified tissue international, 2024-02, Vol.114 (2), p.137-146

2024

Volltextzugriff (PDF)

Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis

Neuroendocrinology, 2022-02, Vol.112 (2), p.186-195

2022

Volltextzugriff (PDF)

Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature

Clinical endocrinology (Oxford), 2023-03, Vol.98 (3), p.383-393

2023

Volltextzugriff (PDF)

Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review

Calcified tissue international, 2023-04, Vol.112 (4), p.483-492

2023

Volltextzugriff (PDF)

Giant prolactinoma in children and adolescents: a single-center experience and systematic review

Pituitary, 2022-12, Vol.25 (6), p.819-830

2022

Volltextzugriff (PDF)

Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review

Clinical endocrinology (Oxford), 2022-12, Vol.97 (6), p.804-813

2022

Volltextzugriff (PDF)

Diagnostic performance of various imaging modalities in localizing ectopic ACTH syndrome: A systematic review

Annales d'endocrinologie, 2024-07

2024

Volltextzugriff (PDF)

Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia

Journal of bone and mineral metabolism, 2024-03, Vol.42 (2), p.155-165

2024

Volltextzugriff (PDF)

Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review

Pituitary, 2024-08, Vol.27 (4), p.335-344

2024

Volltextzugriff (PDF)

GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review

Neuroendocrinology, 2022-08, Vol.112 (8), p.723-732

2022

Volltextzugriff (PDF)

Giant prolactinoma in Asian-Indians: A single-center experience from Western India

Annales d'endocrinologie, 2023-12, Vol.84 (6), p.711-718

2023

Volltextzugriff (PDF)

Renal manifestations of primary hyperparathyroidism

Indian journal of endocrinology and metabolism, 2012-03, Vol.16 (2), p.258-262

2012

Volltextzugriff (PDF)

46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters

Annales d'endocrinologie, 2024-02, Vol.85 (1), p.48-55

2024

Volltextzugriff (PDF)

Homozygous p.Val89Leu plays an important pathogenic role in 5α-reductase type 2 deficiency patients with homozygous p.Arg246Gln in SRD5A2

European journal of endocrinology, 2020-09, Vol.183 (3), p.275

2020

Volltextzugriff (PDF)

Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review

Pituitary, 2022-06, Vol.25 (3), p.444-453

2022

Volltextzugriff (PDF)

Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India

Sexual development, 2021-09, Vol.15 (4), p.253-261

2021

Volltextzugriff (PDF)

LHCGR inactivating variants: single center experience and systematic review of phenotype-genotype of 46,XY and 46,XX patients

Endocrine Connections, 2024-08

2024

Volltextzugriff (PDF)

17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Journal of the Endocrine Society, 2022-03, Vol.6 (3), p.bvac011-bvac011

2022

Volltextzugriff (PDF)

17[alpha]-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Journal of the Endocrine Society, 2022-03, Vol.6 (3)

2022

Volltextzugriff (PDF)

1 – 25 von 29

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(27)
Mit Volltextzugriff
(25)

Publikationsform

Artikel
(28)
Berichte
(1)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Efficacy and safety of burosumab compared with conventional therapy in patients with X-linked hypophosphatemia: A systematic review

177Lu-DOTATATE therapy in metastatic/inoperable pheochromocytoma-paraganglioma

Predictors of Chronic LH-Testosterone Axis Suppression in Male Macroprolactinomas With Normoprolactinemia on Cabergoline

Metastatic cluster 2-related pheochromocytoma/paraganglioma: a single-center experience and systematic review

Vitamin D deficiency or resistance and hypophosphatemia

Pediatric Macrocorticotropinoma: Do They Differ from Microcorticotropinoma?

Hereditary Hypophosphatemic Rickets with Hypercalciuria Presenting with Enthesopathy, Renal Cysts, and High Serum c-Terminal FGF23: Single-Center Experience and Systematic Review

Early Pulse Glucocorticoid Therapy and Improved Hormonal Outcomes in Primary Hypophysitis

Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature

Genotypic Spectrum and its Correlation with Alopecia and Clinical Response in Hereditary Vitamin D Resistant Rickets: Our Experience and Systematic Review

Giant prolactinoma in children and adolescents: a single-center experience and systematic review

Genetic spectrum of Kallmann syndrome: Single‐center experience and systematic review

Diagnostic performance of various imaging modalities in localizing ectopic ACTH syndrome: A systematic review

Inherited Fanconi renotubular syndromes: unveiling the intricacies of hypophosphatemic rickets/osteomalacia

Pituitary apoplexy in cushing’s disease: a single center study and systematic literature review

GNRH1 Variants in Congenital Hypogonadotropic Hypogonadism: Single-Center Experience and Systematic Literature Review

Giant prolactinoma in Asian-Indians: A single-center experience from Western India

Renal manifestations of primary hyperparathyroidism

46,XX aromatase deficiency: A single-center experience with the varied spectrum and recurrent variants, and a systematic review of hormonal parameters

Homozygous p.Val89Leu plays an important pathogenic role in 5α-reductase type 2 deficiency patients with homozygous p.Arg246Gln in SRD5A2

Regional genotypic variations in normosmic congenital hypogonadotropic hypogonadism: our experience and systematic review

Clinical, Hormonal, Genetic, and Molecular Characteristics in Androgen Insensitivity Syndrome in an Asian Indian Cohort from a Single Centre in Western India

LHCGR inactivating variants: single center experience and systematic review of phenotype-genotype of 46,XY and 46,XX patients

17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

17[alpha]-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

Suchergebnisse filtern