Cargando…

Endocrine Disorders Are Prominent Clinical Features in Patients With Primary Antibody Deficiencies

Background: Primary antibody deficiencies (PADs) and anterior pituitary dysfunction are both rare conditions. However, recent studies have remarkably reported the occurrence of anterior pituitary dysfunction in PAD patients. Methods: In this cross-sectional, single-center study we evaluated the prev...

Descripción completa

Detalles Bibliográficos
Autores principales:	Coopmans, Eva C., Chunharojrith, Paweena, Neggers, Sebastian J. C. M. M., van der Ent, Marianne W., Swagemakers, Sigrid M. A., Hollink, Iris H., Barendregt, Barbara H., van der Spek, Peter J., van der Lely, Aart-Jan, van Hagen, P. Martin, Dalm, Virgil A. S. H.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Frontiers Media S.A. 2019
Materias:	Immunology
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6730260/ https://www.ncbi.nlm.nih.gov/pubmed/31543881 http://dx.doi.org/10.3389/fimmu.2019.02079

Ejemplares similares

Approach to the Patient With Treatment-resistant Acromegaly
por: Coopmans, Eva C, et al.
Publicado: (2022)

The position of combined medical treatment in acromegaly
por: Coopmans, Eva C., et al.
Publicado: (2019)

Pegvisomant for acromegaly: does it always works?
por: Neggers, Sebastian J., et al.
Publicado: (2019)

The 11q Terminal Deletion Disorder Jacobsen Syndrome is a Syndromic Primary Immunodeficiency
por: Dalm, Virgil A. S. H., et al.
Publicado: (2015)

Pregnancy and acromegaly
por: Muhammad, Ammar, et al.
Publicado: (2016)

A CDC42 Stop-loss Mutation in a Patient with Relapsing Polychondritis and Autoinflammation
por: van Wijck, Rogier T. A., et al.
Publicado: (2022)

Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency
por: Suratannon, Narissara, et al.
Publicado: (2020)

Metabolic alterations due to IDH1 mutation in glioma: opening for therapeutic opportunities?
por: N Mustafa, Dana A, et al.
Publicado: (2014)

Soluble Klotho: a possible predictor of quality of life in acromegaly patients
por: Coopmans, Eva C., et al.
Publicado: (2020)

A Novel Heterozygous Mutation in the STAT1 SH2 Domain Causes Chronic Mucocutaneous Candidiasis, Atypically Diverse Infections, Autoimmunity, and Impaired Cytokine Regulation
por: Meesilpavikkai, Kornvalee, et al.
Publicado: (2017)

The potential role of biomarkers in predicting gestational diabetes
por: Brink, Huguette S, et al.
Publicado: (2016)

Towards an Earlier Diagnosis of Acromegaly and Gigantism
por: Sisco, Jill, et al.
Publicado: (2021)

Transition readiness among adolescents with rare endocrine conditions
por: van Alewijk, Lisette, et al.
Publicado: (2021)

Marked Reduction of AKT1 Expression and Deregulation of AKT1-Associated Pathways in Peripheral Blood Mononuclear Cells of Schizophrenia Patients
por: van Beveren, Nico J. M., et al.
Publicado: (2012)

Safety of preoperative carvedilol in a patient with recent atenolol-induced pheochromocytoma crisis and cardiomyopathy: A case report
por: Wannachalee, Taweesak, et al.
Publicado: (2020)

Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome
por: van Beveren, Nico J. M., et al.
Publicado: (2012)

Integrative Analysis of Proteomics and DNA Methylation in Orbital Fibroblasts From Graves’ Ophthalmopathy
por: Virakul, Sita, et al.
Publicado: (2021)

Circulating angiogenic cells in glioblastoma: toward defining crucial functional differences in CAC-induced neoplastic versus reactive neovascularization
por: Huizer, Karin, et al.
Publicado: (2020)

Overweight and obesity in type 1 diabetes is not associated with higher ghrelin concentrations
por: Özcan, Behiye, et al.
Publicado: (2021)

Soluble Interleukin-2 Receptor Is a Promising Serum Biomarker for Granulomatous Disease in Common Variable Immune Deficiency
por: van Stigt, Astrid C., et al.
Publicado: (2021)

Microarray and Morphological Analysis of Early Postnatal CRB2 Mutant Retinas on a Pure C57BL/6J Genetic Background
por: Alves, Celso Henrique, et al.
Publicado: (2013)

The role of AIP variants in pituitary adenomas and concomitant thyroid carcinomas in the Netherlands: a nationwide pathology registry (PALGA) study
por: Coopmans, E. C., et al.
Publicado: (2020)

Unacylated Ghrelin Rapidly Modulates Lipogenic and Insulin Signaling Pathway Gene Expression in Metabolically Active Tissues of GHSR Deleted Mice
por: Delhanty, Patric J. D., et al.
Publicado: (2010)

Unacylated ghrelin modulates circulating angiogenic cell number in insulin-resistant states
por: Özcan, Behiye, et al.
Publicado: (2017)

Combined treatment of somatostatin analogues with pegvisomant in acromegaly
por: Franck, S. E., et al.
Publicado: (2015)

OR24-02 Identification of Membrane Proteins That Enhance the Responsiveness of the Ghrelin Receptor
por: Prins, Karina, et al.
Publicado: (2020)

Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome
por: van Beveren, Nico J. M., et al.
Publicado: (2012)

ACRODAT® and AcroVoice: an insight into a holistic approach to the management of acromegaly
por: Lundie, Mark, et al.
Publicado: (2019)

A rare case of ectopic ACTH syndrome caused by primary renal neuroendocrine tumor
por: Chunharojrith, Paweena, et al.
Publicado: (2021)

Associations Between Fatigue and Endocrine and Non-endocrine Health Problems in Turner Syndrome: Cohort Study and Review
por: Rosenberg, Anna G W, et al.
Publicado: (2023)

Determinants of Serum Immunoglobulin Levels: A Systematic Review and Meta-Analysis
por: Khan, Samer R., et al.
Publicado: (2021)

Obesity Is Underestimated Using Body Mass Index and Waist-Hip Ratio in Long-Term Adult Survivors of Childhood Cancer
por: Blijdorp, Karin, et al.
Publicado: (2012)

Comment on Moriconi et al. Very-Low-Calorie Ketogenic Diet as a Safe and Valuable Tool for Long-Term Glycemic Management in Patients with Obesity and Type 2 Diabetes. Nutrients 2021, 13, 758
por: Berk, Kirsten A., et al.
Publicado: (2021)

FRI456 Endocrine and Non-Endocrine Causes of Fatigue in Adults With Turner Syndrome: Cohort Study and Review of the Literature
por: Rosenberg, Anna G W, et al.
Publicado: (2023)

Subclavian artery stenosis caused by a prominent first rib
por: Claus, Isabelle, et al.
Publicado: (2015)

Whole exome sequencing of patients with varicella-zoster virus and herpes simplex virus induced acute retinal necrosis reveals rare disease-associated genetic variants
por: Heinz, Johanna L., et al.
Publicado: (2023)

Molecular clustering of genes related to the atopic syndrome: Towards a more tailored approach and personalized medicine?
por: de Wit, Jill, et al.
Publicado: (2019)

Ten Prominent Host Proteases in Plant-Pathogen Interactions
por: Thomas, Emma L., et al.
Publicado: (2018)

Chronically Activated T-cells Retain Their Inflammatory Properties in Common Variable Immunodeficiency
por: Berbers, Roos-Marijn, et al.
Publicado: (2021)

Three patients with defects in interferon gamma receptor signaling: A challenging diagnosis
por: Zhou, Zijun, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_k3nsqprfpgjfi73uv022amu7pr