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Mononeuropathy Multiplex

Known as: Mononeuropathy Multiplex Syndromes, Mononeuropathy Multiplex Syndrome, Syndromes, Mononeuropathy Multiplex 
National Institutes of Health

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Mononeuropathies

Papers overview

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2008
2008
Detection of genetically modified crops by combination of multiplex PCR and low-density DNA microarray.
2007
2007
Virus detection and identification using random multiplex (RT)-PCR with 3'-locked random primers
BackgroundPCR-based detection and identification of viruses assumes a known, relatively stable genome. Unfortunately, high… 
2007
2007
[Detection of allergenic substances in foods by a multiplex PCR method].
A multiplex PCR (M-PCR) method was developed for the detection of DNAs of plant and three allergenic substances (wheat, buckwheat… 
2007
2007
Evaluation of a Multiplex PCR for Identification of Enteroaggregative Escherichia coli
Enteroaggregative Escherichia coli (EAEC) has emerged as an important pathogen associated with endemic and epidemic diarrheal… 
2006
2006
A rapid and simple system of detecting deletions on the Y chromosome related with male infertility using multiplex PCR.
Around 10% of males with idiopathic azoospermia or oligozoospermia, which are important causes of male infertility, have partial… 
2003
2003
Motor‐axonal polyneuropathy associated with hepatitis C virus
The association between hepatitis C virus (HCV) infection, the presence of mixed cryoglobulinemia and peripheral neuropathy is… 
2002
2002
Forward error correcting codes in fiber-optic synchronous code-division multiple access networks
2001
2001
Prenatal diagnosis of Pelizaeus‐Merzbacher disease: detection of proteolipid protein gene duplication by quantitative fluorescent multiplex PCR
A prenatal diagnosis of Pelizaeus‐Merzbacher disease (PMD) resulting from proteolipid protein gene (PLP) duplication was… 
1999
1999
Four common mutations of the cystathionine beta-synthase gene detected by multiplex PCR and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
BACKGROUND A deficiency of cystathionine beta-synthase (CBS) is the most frequent cause of homocystinuria. The effect of therapy… 
1996
1996
Diagnosis of multiple endocrine neoplasia [MEN] 2A, 2B and familial medullary thyroid cancer [FMTC] by multiplex PCR and heteroduplex analyses of RET proto‐oncogene mutations
Multiple endocrine neoplasia type 2 [MEN 2] is an autosomal dominant cancer syndrome with two subtypes, 2A and 2B. MEN 2A and… 
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