Results 41 to 50 of about 2,206,205 (317)

Акне як прояв дисбіозу кишечника [PDF]

, 2011
У больных угревой болезнью степень тяжести ее проявлений значительно увеличивается при наличии кишечных синдромов (раздраженного кишечника, маль-абсорбции).
Корецька, О.Ю.
core   +2 more sources

A novel familial mutation in the PCSK1 gene that alters the oxyanion hole residue of proprotein convertase 1/3 and impairs its enzymatic activity. [PDF]

, 2014
Four siblings presented with congenital diarrhea and various endocrinopathies. Exome sequencing and homozygosity mapping identified five regions, comprising 337 protein-coding genes that were shared by three affected siblings. Exome sequencing identified
Abbasi, Montaser, Bar-Oz, Benjamin, Berger, Itai, Blanco, Elias, Elpeleg, Orly, Lindberg, Iris, Martín, Martin G, Pappo, Orit, Shteyer, Eyal, Wilschanski, Michael, Yourshaw, Michael, Zangen, David   +11 more
core   +2 more sources

On the Question of Differential Diagnosis of Malabsorption Syndromes (lactase insufficiency, gluten intolerance, celiac disease)

Gastroenterologìa, 2015
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D.I. Kvit, T.Z. Marchenko, Ya.V. Tomkiv, H.Z. Vivcharivska, V.D. Shaidych, L.V. Zastavna, L.M. Horaiska, L.P. Sakalosh, Z.V. Tomkiv   +8 more
doaj   +1 more source

Autoimmune polyglandular syndromes

Лечащий Врач, 2023
Autoimmune polyendocrine syndromes (APS) are a group of syndromes characterized by autoimmune damage of two or more endocrine glands, leading most often to their hypofunction.
V. V. Smirnov, I. D. Gurova
doaj   +1 more source

A case of superior mesenteric artery syndrome

Radiology Case Reports, 2022
Superior mesenteric artery (SMA) syndrome, also known as Cast syndrome, Wilkie's syndrome, or duodenal ileus, is a rare condition involving compression of the duodenum between the aorta and the SMA, primarily attributed to loss of the intervening ...
Shiavax J Rao, MD, Pallavi Lakra, MBBS, Kalyan Paudel, MD, Christopher J Haas, MD, PhD   +3 more
doaj  

Neuroacanthocytosis Syndromes

Orphanet Journal of Rare Diseases, 2011
Neuroacanthocytosis (NA) syndromes are a group of genetically defined diseases characterized by the association of red blood cell acanthocytosis and progressive degeneration of the basal ganglia.
Walker Ruth H, Danek Adrian, Jung Hans H
doaj   +1 more source

Outer retina changes on optical coherence tomography in vitamin A deficiency

International Journal of Retina and Vitreous, 2020
Background Vitamin A deficiency is rare in the United States and can be missed in patients with malabsorption syndromes without a high dose of suspicion.
Meghan K. Berkenstock, Charles J. Castoro, Andrew R. Carey   +2 more
doaj   +1 more source

Preoperative Vitamin D Supplementation to Reduce Hypocalcemia Following Total Thyroidectomy: Systematic Review and Meta‐Analysis of Randomized Clinical Trials

Head &Neck, EarlyView.
ABSTRACT Objective This study aims to determine whether preoperative supplementation of vitamin D reduces the incidence of hypocalcemia following total thyroidectomy. Methods Conducted in conformity with the PRISMA statement, a systematic review and meta‐analysis of randomized clinical trials (RCT) was performed assessing postoperative hypocalcemia and
Luca Canali, Gian Marco Pace, Marika D. Russell, Francesca Gaino, Luca Malvezzi, Gherardo Mazziotti, Andrea Lania, Giuseppe Spriano, Michael Mannstadt, Gregory W. Randolph, Giuseppe Mercante   +10 more
wiley   +1 more source

Pain in systemic connective tissue diseases [PDF]

, 2015
Pain is frequent in patients with connective tissue diseases (CTDs), particularly those affected by systemic sclerosis (SSc) and systemic lupus erythematosus (SLE) in which it is virtually ubiquitous and can have different causes.
Atzeni, Fabiola, Bazzichi, Laura, Casale, Roberto, DI FRANCO, Manuela, Sarzi Puttini, Piercarlo   +4 more
core   +1 more source

Clinical, hematological, and imaging observations in a 25-year-old woman with abetalipoproteinemia

Annals of Indian Academy of Neurology, 2014
Abetalipoproteinemia is an uncommon cause of ataxia and retinitis pigmentosa (RP). Most of the neurological and ocular manifestations occur secondary to deficiency syndromes that is consequent to fat malabsorption from the small intestine. In this report,
Madhu Nagappa, Parayil S Bindu, Sikandar Adwani, Sangeeta K Seshagiri, Jitender Saini, Sanjib Sinha, Arun B Taly   +6 more
doaj   +1 more source