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Ethically problematic treatment decisions in different medical specialties

Journal of medical ethics, 2008-04, Vol.34 (4), p.262-267

2008

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Spectrum of Mutations in Aspartylglucosaminuria

Proceedings of the National Academy of Sciences - PNAS, 1991-12, Vol.88 (24), p.11222-11226

1991

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Serum procollagen type III is an early and sensitive marker for veno-occlusive disease of the liver in children undergoing bone marrow transplantation

Blood, 1994-05, Vol.83 (10), p.3036-3040

1994

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Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease

The EMBO journal, 1991-01, Vol.10 (1), p.51-58

1991

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The Role of National Ethics Commissions in Finland

Bioethics, 2003-08, Vol.17 (4), p.357-368

Halila, Ritva

2003

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Expanding screening for rare metabolic disease in the newborn : An analysis of costs, effect and ethical consequences for decision-making in Finland

Acta pædiatrica (Oslo), 2005-08, Vol.94 (8), p.1126-1136

2005

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Human leucocyte aspartylglucosaminidase. Evidence for two different subunits in a more complex native structure

Biochemical journal, 1991-05, Vol.276 ( Pt 1) (1), p.251-256

1991

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Purification of human procollagen type III N-proteinase from placenta and preparation of antiserum

Biochemical journal, 1986-10, Vol.239 (1), p.47-52

1986

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Enzymes converting procollagens to collagens

Journal of cellular biochemistry, 1985, Vol.28 (1), p.15-21

1985

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Human aspartylglucosaminidase : a biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts

Biochemical journal, 1992-09, Vol.286 (2), p.613-618

1992

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Neutral protease cleaving the N-terminal propeptide of type III procollagen: partial purification and characterization of the enzyme from smooth muscle cells of bovine aorta

Biochemistry (Easton), 1984-03, Vol.23 (6), p.1251-1256

1984

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The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2p22

Cytogenetic and genome research, 1995-01, Vol.68 (1-2), p.61-63

1995

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Why Shouldn't Children Decide Whether They Are Enrolled in Nonbeneficial Medical Research?

American journal of bioethics, 2003, Vol.3 (4), p.35-36

2003

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Processing of types I and III procollagen in Ehlers-Danlos syndrome type VII

American journal of human genetics, 1986-08, Vol.39 (2), p.222-231

1986

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A sensitive and rapid method for assaying the activity of type III procollagen amino-terminal proteinase

Analytical biochemistry, 1985-02, Vol.145 (1), p.205-211

Halila, Ritva

1985

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Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)

Gene, 1996-09, Vol.174 (1), p.135-143

1996

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N-terminal propeptide of type III collagen in tracheal fluid and serum in preterm infants at risk for bronchopulmonary dysplasia

Pediatric research, 1992-04, Vol.31 (4), p.340-343

1992

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Aspartylglucosaminuria (AGU): Protein and Gene Structure of Normal and Mutated Aspartylglucosaminidase

Biochemical Medicine and Metabolic Biology, 1993-08, Vol.50 (1), p.1-8

1993

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Human leucocyte aspartylglycosaminidase : evidence for two different subunits in a more complex native structure

Biochemical journal, 1991, Vol.276, p.251-256

1991

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Natural Laminar-Flow Airfoil Optimization Design Using a Discrete Adjoint Approach

AIAA journal, 2020-11, Vol.58 (11), p.4702-4722

2020

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Aspartylglucosaminuria : cDNA encoding human aspartylgucosaminidase and the missense mutation causing the disease

The EMBO journal, 1991, Vol.10 (1), p.51-58

1991

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Adjoint-based aerodynamic shape optimization including transition to turbulence effects

Aerospace science and technology, 2020-12, Vol.107, p.106243, Article 106243

2020

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Toward Automatic Parabolized Stability Equation-Based Transition-to-Turbulence Prediction for Aerodynamic Flows

AIAA journal, 2021-02, Vol.59 (2), p.462-473

2021

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The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22

Cytogenetics and cell genetics, 1995, Vol.68 (1-2), p.61

1995

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Sulfated Glycosaminoglycan-Based Block Copolymer: Preparation of Biocompatible Chondroitin Sulfate‑b‑poly(lactic acid) Micelles

Biomacromolecules, 2014-07, Vol.15 (7), p.2691-2700

2014

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Ethically problematic treatment decisions in different medical specialties

Spectrum of Mutations in Aspartylglucosaminuria

Serum procollagen type III is an early and sensitive marker for veno-occlusive disease of the liver in children undergoing bone marrow transplantation

Aspartylglucosaminuria: cDNA encoding human aspartylglucosaminidase and the missense mutation causing the disease

The Role of National Ethics Commissions in Finland

Expanding screening for rare metabolic disease in the newborn : An analysis of costs, effect and ethical consequences for decision-making in Finland

Human leucocyte aspartylglucosaminidase. Evidence for two different subunits in a more complex native structure

Purification of human procollagen type III N-proteinase from placenta and preparation of antiserum

Enzymes converting procollagens to collagens

Human aspartylglucosaminidase : a biochemical and immunocytochemical characterization of the enzyme in normal and aspartylglucosaminuria fibroblasts

Neutral protease cleaving the N-terminal propeptide of type III procollagen: partial purification and characterization of the enzyme from smooth muscle cells of bovine aorta

The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2p22

Why Shouldn't Children Decide Whether They Are Enrolled in Nonbeneficial Medical Research?

Processing of types I and III procollagen in Ehlers-Danlos syndrome type VII

A sensitive and rapid method for assaying the activity of type III procollagen amino-terminal proteinase

Molecular cloning, expression and chromosomal localization of a human gene encoding a 33 kDa putative metallopeptidase (PRSM1)

N-terminal propeptide of type III collagen in tracheal fluid and serum in preterm infants at risk for bronchopulmonary dysplasia

Aspartylglucosaminuria (AGU): Protein and Gene Structure of Normal and Mutated Aspartylglucosaminidase

Human leucocyte aspartylglycosaminidase : evidence for two different subunits in a more complex native structure

Natural Laminar-Flow Airfoil Optimization Design Using a Discrete Adjoint Approach

Aspartylglucosaminuria : cDNA encoding human aspartylgucosaminidase and the missense mutation causing the disease

Adjoint-based aerodynamic shape optimization including transition to turbulence effects

Toward Automatic Parabolized Stability Equation-Based Transition-to-Turbulence Prediction for Aerodynamic Flows

The human gene for xanthine dehydrogenase (XDH) is localized on chromosome band 2q22

Sulfated Glycosaminoglycan-Based Block Copolymer: Preparation of Biocompatible Chondroitin Sulfate‑b‑poly(lactic acid) Micelles

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