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E L Romppanen

Explore the profile of E L Romppanen including associated specialties, affiliations and a list of published articles. Areas
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Articles 8
Citations 16
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Recent Articles
1.
Romppanen E
Scand J Clin Lab Invest . 2001 May; 61(2):123-9. PMID: 11347979
Oligonucleotide ligation assay combined with polymerase chain reaction (PCR-OLA) is a technique which can be used for the detection of characterized sequence variations. In the present study, new PCR-OLA methods...
2.
Romppanen E, Mononen I
Clin Chem . 2000 Jun; 46(6 Pt 1):811-6. PMID: 10839769
Background: Congenital nephrotic syndrome of Finnish type (NPHS1) is an autosomal recessive disorder characterized by severe proteinuria of intrauterine onset. Ninety-four percent of the Finnish NPHS1 chromosomes have been reported...
3.
Romppanen E, Savolainen K, Mononen I
Anal Biochem . 2000 Feb; 279(1):111-4. PMID: 10683239
No abstract available.
4.
Romppanen E, Mononen I
Clin Chem . 1999 Nov; 45(11):2022-5. PMID: 10545079
No abstract available.
5.
Romppanen E, Valtonen P, Mononen T, Mononen I
Clin Chem . 1998 Nov; 44(11):2373-6. PMID: 9799772
No abstract available.
6.
Romppanen E, Mononen T, Mononen I
Clin Chem . 1998 Apr; 44(1):68-71. PMID: 9550560
Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is a recessively inherited defect in the mitochondrial beta-oxidation of fatty acids. A single nucleotide change, the A985 --> G transition, in the MCAD gene...
7.
Mononen I, Heisterkamp N, Dunder U, Romppanen E, Noronkoski T, Kuronen I, et al.
FASEB J . 1995 Mar; 9(5):428-33. PMID: 7896015
Aspartylglycosaminuria (AGU) is the most common disorder of glycoprotein degradation. AGU patients are deficient in glycosylasparaginase (GA), which results in accumulation of aspartylglucosamine in body fluids and tissues. Human glycosylasparaginase...
8.
Pelkonen S, Romppanen E, Siitonen A, Pelkonen J
J Clin Microbiol . 1994 Sep; 32(9):2128-33. PMID: 7529248
We genotyped Salmonella serovar infantis (referred to as S. infantis), which is the most widespread serovar among animals and the third most common cause of human salmonellosis in Finland. Molecular...