Download the Free Prime PubMed App to your smartphone or tablet.

Available for iPhone or iPad:

Unbound PubMed app for iOS iPhone iPadAlso Available:
Unbound MEDLINE
Unbound PubMed app for Android

Available for Mac and Windows Desktops and laptops:

Unbound PubMed app for WindowsUnbound PubMed app for MAC OS Yosemite Macbook Air pro
(suggestive)
68,498 results
  • Nonketotic Hyperglycinemia: Two Case Reports and Review. [Journal Article]
    Neurodiagn J 2019; :1-10Poothrikovil RP, Al Thihli K, … Al Murshidi F
  • Nonketotic hyperglycinemia (NKH) or glycine encephalopathy is an autosomal recessive disorder of glycine metabolism resulting in an excessive accumulation of glycine in all body tissues, including the central nervous system. It is caused by a biochemical defect in the glycine cleavage system and considered as a rare disorder with an estimated prevalence of 1:60,000. The neonatal form presents in …
  • Malakoplakia of the Bladder in a 4-Month-Old Puppy. [Journal Article]
    J Am Anim Hosp Assoc 2019 Sep/Oct; 55(5):261-265Benzimra C, Job C, … R Faucher M
  • A 4 mo old female Staffordshire bull terrier puppy was presented with chronic Escherichia coli cystitis. Ultrasound and cystoscopic examination revealed innumerable, intraluminal, finger-like proliferations arising from the dorsal urinary bladder (UB) wall. Histological examination of mucosal biopsies obtained by cystoscopy was suggestive of granulomatous cystitis. The proliferative lesions were …
  • Association of FCRL3 Gene Polymorphisms with IgA Nephropathy in a Chinese Han Population. [Journal Article]
    DNA Cell Biol 2019Zhong Z, Feng S, … Li M
  • Our previous genome-wide association study has identified a suggestive association at rs11264799 within FCRL3 (Fc receptor-like 3) locus on 1q23.1 for IgA nephropathy (IgAN) in a Chinese Han population. This study aims to investigate the association of FCRL3 variants with the susceptibility, clinicopathological phenotypes and prognosis of IgAN. Eleven FCRL3 single-nucleotide polymorphisms (SNPs) …
  • Macrophage Activation Syndrome Secondary to Underlying Sarcoidosis. [Case Reports]
    Cureus 2019; 11(6):e4929Kasparian S, Anand K, … Pingali SRK
  • Hemophagocytic lymphohistiocytosis (HLH) due to an underlying rheumatologic condition is known as macrophage activation syndrome (MAS), a rare and serious complication that often has a delayed diagnosis. MAS can complicate any rheumatologic disease, although it is most prevalent in systemic juvenile idiopathic arthritis. MAS occurring as a sequela of sarcoidosis is seldom reported. Herein, we pre…
New Search Next