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Probing Single-Cell Macrophage Polarization and Heterogeneity Using Thermo-Reversible Hydrogels in Droplet-Based Microfluidics

Frontiers in bioengineering and biotechnology, 2021-10, Vol.9, p.715408-715408

2021

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Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidation

Journal of inherited metabolic disease, 1990-05, Vol.13 (3), p.311-314

1990

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Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis

European journal of pediatrics, 1988-11, Vol.148 (2), p.126-131

1988

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3-hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death : protective effect of medium-chain triglyceride treatment

European journal of pediatrics, 1991, Vol.150 (3), p.190-195

1991

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Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method : the effect of oral riboflavin supplementation

Pediatric research, 1992, Vol.31 (1), p.39-42

1992

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β‐Mannosidosis in two brothers with hearing loss

Journal of inherited metabolic disease, 1988-06, Vol.11 (S2), p.255-258

1988

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SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE

The Lancet (British edition), 1989-07, Vol.334 (8653), p.52-53

1989

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Novel storage products in humanβ‐mannosidosis

Journal of inherited metabolic disease, 1990-05, Vol.13 (3), p.273-276

1990

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Rapid diagnosis of 3-hydroxy-3-methylglutaryl—coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method

Clinica chimica acta, 1990-08, Vol.189 (3), p.327-334

1990

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3-methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme a hydratase is normal

European journal of pediatrics, 1988-10, Vol.148 (1), p.76-82

1988

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The cerebro-costo-mandibular syndrome: third report of familial occurrence

Clinical genetics, 1985-08, Vol.28 (2), p.118-121

1985

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A patient with sarcosinaemia

Journal of inherited metabolic disease, 1986-12, Vol.9 (4), p.404-405

1986

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New defects of pyrimidine metabolism

Advances in experimental medicine and biology, 1984, Vol.165 Pt A, p.109

1984

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Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine

Clinica chimica acta, 1983-05, Vol.130 (2), p.231-238

1983

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Nϵ-(carboxymethyd)lysine, a constituent of human urine

Clinica chimica acta, 1975-03, Vol.59 (3), p.313-320

1975

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Chromatographic determination and mass spectrometric identification of γ-glutamylphenylalanine, a urinary constituent in phenylketonuria

Clinica chimica acta, 1980-03, Vol.102 (2), p.137-145

1980

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Tyrosinosis

Nederlands tijdschrift voor geneeskunde, 1976-05, Vol.120 (22), p.944

1976

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A case of formiminoglutamic aciduria. Clinical and biochemical studies

European journal of pediatrics, 1981-07, Vol.136 (3), p.319-323

1981

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Letter: Possible hazards of neomycin treatment in methylmalonic acidemia

Pediatrics (Evanston), 1974-05, Vol.53 (5), p.765

1974

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Tyrosinemia and tyrosyluria in healthy prematures: Time courses not vitamin C-dependent

Clinica chimica acta, 1975-05, Vol.61 (1), p.73-90

1975

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Dietary correction of histidinemia in older children possible

Clinica chimica acta, 1973-12, Vol.49 (3), p.377-382

1973

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Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normals

Clinica chimica acta, 1971, Vol.31 (1), p.215-224

1971

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Fructose-1,6-diphosphatase deficiency: Another enzyme defect which can present itself with the clinical features of “tyrosinosis”

Clinica chimica acta, 1974-08, Vol.55 (1), p.41-47

1974

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Computer analysis of the EEG as an aid in terminating diet therapy in phenylketonuria

Revue d'électroencéphalographie et de neurophysiologie clinique, 1978-01, Vol.8 (1), p.55-60

1978

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Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria

Electroencephalography and clinical neurophysiology, 1979-01, Vol.46 (2), p.205-213

1979

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Probing Single-Cell Macrophage Polarization and Heterogeneity Using Thermo-Reversible Hydrogels in Droplet-Based Microfluidics

Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidation

Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis

3-hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death : protective effect of medium-chain triglyceride treatment

Diagnosis of medium-chain acyl-CoA dehydrogenase deficiency in lymphocytes and liver by a gas chromatographic method : the effect of oral riboflavin supplementation

β‐Mannosidosis in two brothers with hearing loss

SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASE

Novel storage products in humanβ‐mannosidosis

Rapid diagnosis of 3-hydroxy-3-methylglutaryl—coenzyme A lyase deficiency via enzyme activity measurements in leukocytes or platelets using a simple spectrophotometric method

3-methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme a hydratase is normal

The cerebro-costo-mandibular syndrome: third report of familial occurrence

A patient with sarcosinaemia

New defects of pyrimidine metabolism

Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine

Nϵ-(carboxymethyd)lysine, a constituent of human urine

Chromatographic determination and mass spectrometric identification of γ-glutamylphenylalanine, a urinary constituent in phenylketonuria

Tyrosinosis

A case of formiminoglutamic aciduria. Clinical and biochemical studies

Letter: Possible hazards of neomycin treatment in methylmalonic acidemia

Tyrosinemia and tyrosyluria in healthy prematures: Time courses not vitamin C-dependent

Dietary correction of histidinemia in older children possible

Automatic column chromatographic analysis of urinary and serum imidazoles in patients with histidinaemia and normals

Fructose-1,6-diphosphatase deficiency: Another enzyme defect which can present itself with the clinical features of “tyrosinosis”

Computer analysis of the EEG as an aid in terminating diet therapy in phenylketonuria

Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria

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