Results 211 to 220 of about 399,679 (248)
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Sanfilippo syndrome: A mini‐review

Journal of Inherited Metabolic Disease, 2008
SummaryMucopolysaccharidosis type III (MPS III, Sanfilippo syndrome) is an autosomal recessive disorder, caused by a deficiency in one of the four enzymes involved in the lysosomal degradation of the glycosaminoglycan heparan sulfate. Based on the enzyme deficiency, four different subtypes, MPS IIIA, B, C, and D, are recognized.
Valstar, M. J.   +4 more
openaire   +3 more sources

Hemodiafiltration: A Mini Review

American Journal of Kidney Diseases
Hemodialysis allows people with kidney failure to survive vital organ failure; however, most do not recover premorbid functional status. Despite early efforts focused on increased removal of small molecular weight solutes, high levels of morbidity and mortality persist due to the condition underlying kidney failure, co-morbid medical conditions, and ...
Jonathan T. Lin, Jeffrey I. Silberzweig
openaire   +2 more sources

Mini‐reviews

BJU International, 2005
Khurshid R, Ghani   +2 more
openaire   +2 more sources

Mini Review

2021
Aastha Paliwal   +2 more
openaire   +1 more source

Mini-Review

Hispanic Journal of Behavioral Sciences, 1982
openaire   +2 more sources

MINI REVIEW

Human Reproduction, 1991
Seth Granberg, Mats Wikland
openaire   +1 more source

Reliability and validity of Japanese version of the Mini‐International Neuropsychiatric Interview

Psychiatry and Clinical Neurosciences, 2005
Tempei Otsubo   +2 more
exaly  

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