Cargando…

Two birds one stone: semaglutide is highly effective against severe psoriasis in a type 2 diabetic patient

SUMMARY: Semaglutide is a glucagon-like peptide 1 (GLP-1) receptor agonist, approved for the treatment of type 2 diabetes mellitus (T2DM). GLP-1 analogs exert several biological activities connected not only with an insulinotropic effect but also with immunoregulation and reduction of inflammation....

Descripción completa

Detalles Bibliográficos
Autores principales:	Costanzo, Gabriele, Curatolo, Salvatore, Busà, Barbara, Belfiore, Antonino, Gullo, Damiano
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Bioscientifica Ltd 2021
Materias:	Insight into Disease Pathogenesis or Mechanism of Therapy
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8428016/ https://www.ncbi.nlm.nih.gov/pubmed/34463640 http://dx.doi.org/10.1530/EDM-21-0007

Ejemplares similares

Vanishing hypercalciuric kidney stones after treating underlying acromegaly
por: van der Valk, Eline, et al.
Publicado: (2013)

Insulin autoimmune syndrome: not just one but two different diseases with therapeutic implications
por: Wammer, Anne Cathrine Parelius, et al.
Publicado: (2023)

A clinically novel AIP mutation in a patient with a very large, apparently sporadic somatotrope adenoma
por: Salvatori, Roberto, et al.
Publicado: (2014)

The dilemma of the gender assignment in a Portuguese adolescent with disorder of sex development due to 17β-hydroxysteroid-dehydrogenase type 3 enzyme deficiency
por: Costa, Carla, et al.
Publicado: (2014)

Bilateral adrenal gland haemorrhage: an unusual cause
por: Gowda, Durgesh, et al.
Publicado: (2014)

Pituitary metastases from papillary carcinoma of thyroid: a case report and literature review
por: Chikani, Viral, et al.
Publicado: (2013)

First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene
por: Casey, R, et al.
Publicado: (2013)

Identification of a novel heterozygous mutation in exon 50 of the COL1A1 gene causing osteogenesis imperfecta
por: Aftab, S A S, et al.
Publicado: (2013)

Radioiodine treatment of differentiated thyroid cancer despite history of ‘iodine allergy’
por: Puchalski, Adam R, et al.
Publicado: (2014)

Tumor-induced osteomalacia due to a recurrent mesenchymal tumor overexpressing several growth factor receptors
por: Yavropoulou, Maria P, et al.
Publicado: (2015)

Autoimmune alternating hyper- and hypo-thyroidism: a rare condition in pediatrics
por: Martins, Luísa Correia, et al.
Publicado: (2016)

Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene
por: Nobel, Yael R, et al.
Publicado: (2016)

Successful fertility treatment with gonadotrophin therapy for male hypogonadotrophic hypogonadism
por: Rajkanna, J, et al.
Publicado: (2016)

Asymptomatic Paget's disease of bone in a 62-year-old Nigerian man: three years post-alendronate therapy
por: Aransiola, Clement Olukayode, et al.
Publicado: (2016)

Heterogeneity of glucagonomas due to differential processing of proglucagon-derived peptides
por: Challis, Benjamin G, et al.
Publicado: (2015)

Xanthogranulomatous hypophysitis: a rare and often mistaken pituitary lesion
por: Gopal-Kothandapani, Jaya Sujatha, et al.
Publicado: (2015)

Pancreas-protective effect of rituximab for acute-onset type 1 diabetes in the honeymoon period: a case report
por: Kurozumi, Akira, et al.
Publicado: (2016)

Lipoid congenital adrenal hyperplasia due to STAR mutations in a Caucasian patient
por: Kaur, Jasmeet, et al.
Publicado: (2016)

A novel immunopathological association of IgG4-RD and vasculitis with Hashimoto's thyroiditis
por: Minamino, Hiroto, et al.
Publicado: (2016)

Gonadotropin-releasing hormone agonist-induced pituitary apoplexy
por: Keane, Fergus, et al.
Publicado: (2016)

Thyroid antibody-negative euthyroid Graves’ ophthalmopathy
por: Tabasum, Arshiya, et al.
Publicado: (2016)

Adrenal cancer in neurofibromatosis type 1: case report and DNA analysis
por: Menon, Ravi Kumar, et al.
Publicado: (2014)

Impact of a novel 14 bp MEN1 deletion in a patient with hyperparathyroidism and gastrinoma
por: Birla, Shweta, et al.
Publicado: (2015)

Transient diabetes insipidus in pregnancy
por: Marques, Pedro, et al.
Publicado: (2015)

Cushing's storm secondary to a rare case of ectopic ACTH secreting metastatic breast cancer
por: Bucciarelli, Maura, et al.
Publicado: (2015)

Resistant hypertension with adrenal nodule: are we removing the right gland?
por: Das, Gautam, et al.
Publicado: (2015)

Follicular thyroid carcinoma with NRAS Q61K and GNAS R201H mutations that had a good (131)I treatment response
por: Lu, Jin-Ying, et al.
Publicado: (2016)

Management of metastatic thyroid cancer in pregnancy: risk and uncertainty
por: Rowe, Christopher W, et al.
Publicado: (2016)

Flying under the radar: treatment of refractory hyperglycemia
por: Kandel, S M, et al.
Publicado: (2016)

Insulin Autoimmune Syndrome: a rare cause of postprandial hypoglycemia
por: Sahni, Pooja, et al.
Publicado: (2016)

Novel SCC mutation in a patient of Mexican descent with sex reversal, salt-losing crisis and adrenal failure
por: Kaur, Jasmeet, et al.
Publicado: (2016)

Refractory hypoglycemia in a patient with functional adrenal cortical carcinoma
por: Marchetti, Katia Regina, et al.
Publicado: (2016)

Autoimmune polyendocrinopathy and hypophysitis after Puumala hantavirus infection
por: Tarvainen, Marlene, et al.
Publicado: (2016)

Growth of a progesterone receptor-positive meningioma in a female patient with congenital adrenal hyperplasia
por: O’Shea, T, et al.
Publicado: (2016)

Brown tumor of the jaw after pregnancy and lactation in a MEN1 patient
por: Casteràs, Anna, et al.
Publicado: (2016)

Pancreatic α-cell hyperplasia and hyperglucagonemia due to a glucagon receptor splice mutation
por: Larger, Etienne, et al.
Publicado: (2016)

Clinical challenges in the management of isolated GH deficiency type IA in adulthood
por: Casteràs, Anna, et al.
Publicado: (2014)

Cured primary hyperparathyroidism after fine-needle aspiration biopsy-induced parathyroid disappearance
por: Kara, Elda, et al.
Publicado: (2017)

A rare cause of primary adrenal insufficiency due to a homozygous Arg188Cys mutation in the STAR gene
por: Burget, Lukas, et al.
Publicado: (2018)

Growth trajectory and pubertal tempo from birth till final height in a girl with Wolf-Hirschhorn syndrome
por: Siew, Jia Xuan, et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_6o20644el52fqq33a02u633kev