Results 71 to 80 of about 1,158,693 (154)
Proteus Syndrome: Description of Two Clinical Cases
Вопросы современной педиатрииBackground. Proteus syndrome is extremely rare congenital multisystem disease with high variability in clinical manifestations. Its prevalence is unknown, there are less than 200 cases in the world literature. The syndrome is a classic example of somatic
Tatiana S. Belysheva +13 more
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POEMS Syndrome: 2026 Update on Diagnosis, Risk‐Stratification, and Management
American Journal of Hematology, Volume 101, Issue 10, Page 2632-2651, October 2026.ABSTRACT Disease Overview POEMS syndrome is a life‐threatening syndrome due to an underlying plasma cell neoplasm. The major criteria for the syndrome are polyneuropathy, clonal plasma cell disorder (PCD), sclerotic bone lesions, elevated vascular endothelial growth factor, and the presence of Castleman disease.
Angela Dispenzieri
wiley +1 more source
Macrodactyly and proteus syndrome
, 2006 Macrodactyly is a rare congenital, nonhereditary malformation presenting as an increased size of one or several digits of the hands or feet. Proteus syndrome, consisting of various clinical manifestations, is a congenital hamartomatous syndrome involving
Özdemir, Özmert Muhammet Ali +2 more
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Hemimegalencephaly: A Foetal Tauopathy
Pediatric Neurology Briefs, 2013 Researchers at University of Calgary and Alberta Children's Hospital, Canada; and University of Pennsylvania, Philadelphia studied brain resections from 3 male infants with hemimegalencephaly (HME) and refractory epilepsy.
J Gordon Millichap
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Chemistry &Biodiversity, Volume 23, Issue 9, September 2026.This review majorly describes the systematic development of Akt inhibitors involving numerous heterocyclic scaffolds along with their structure activity relationships to explore anticancer therapeutic strategies. ABSTRACT The Akt pathway is dysregulated in cancer, leading to proliferation, decreased apoptosis, and metastasis, and hence is a major ...
Mayur S. Dhangar, Mahesh B. Palkar
wiley +1 more source
De Novo PTEN Mutation in a Young Boy with Cutaneous Vasculitis
Case Reports in Pediatrics, 2017 Phosphatase and tensin homolog (PTEN) is the protein encoded by the PTEN gene (10q23.3). PTEN mutations are related to a variety of rare diseases referred to collectively as PTEN hamartoma tumor syndromes (PHTS), which include Cowden Syndrome, Bannayan ...
Angela Mauro +4 more
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Proteus syndrome: Clinical diagnosis of a series of cases
Indian Journal of Endocrinology and Metabolism, 2013 Objectives: This paper describes the clinical diagnosis of Proteus syndrome (PS) in children referred for evaluation of asymmetric disproportionate overgrowth.
Cresio Alves +2 more
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Journal of Clinical Laboratory Analysis, Volume 40, Issue 18, September 2026.Schematic overview of the human microbiome and major microbiota‐derived metabolites across body sites, highlighting the gut–brain, gut–heart, and gut–kidney axes in host physiology and disease. ABSTRACT Background The human microbiome is a dynamic and diverse community of microorganisms that affects susceptibility to illness and promotes wellness ...
Awadh Alanazi
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Journal of Orthopaedic Research, Volume 44, Issue 9, September 2026.ABSTRACT Ischemia‐reperfusion injury (IRI) induces skeletal muscle damage through oxidative stress, impaired autophagy, and satellite cell (SC) dysfunction, ultimately compromising regenerative capacity and functional recovery. We investigated whether the naturally occurring autophagy‐stimulating compound 2‐n‐hexyl lanthionine ketenamine phosphonate (2‐
Valentina Barrera +7 more
wiley +1 more source
Severe anal bleeding in Proteus syndrome: a case report [PDF]
, 2007 Proteus syndrome was originally described by Cohen and Hayden in 1979. The disorder was named Proteus syndrome by Wiedmann and colleagues in 1983 after Proteus, the giant Greek god of the sea.
J. M. L. G. Gehlen +7 more
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