Newborn urine screening experience with over one million infants in the Quebec Network of Genetic Medicine (Q70384330)

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10 October 2019

title

Newborn urine screening experience with over one million infants in the Quebec Network of Genetic Medicine (English)

1 reference

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10 October 2019

author name string

B Lemieux

1

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10 October 2019

C Auray-Blais

2

1 reference

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10 October 2019

R Giguère

3

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10 October 2019

D Shapcott

4

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10 October 2019

C R Scriver

5

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10 October 2019

publication date

1 January 1988

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Journal of Inherited Metabolic Disease

10 October 2019

published in

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10 October 2019

volume

11

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10 October 2019

issue

1

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10 October 2019

page(s)

45-55

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https://scigraph.springernature.com/pub.10.1007/bf01800056

10 October 2019

exact match

0 references

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12 December 2020

Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria

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Diet and medications giving positive ninhydrin reactions on TLC in a newborn urinary screening program

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12 December 2020

A filter paper sampling method for the uric acid:creatinine ratio in urine. Normal values in the the newborn

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12 December 2020

Outcome of early and long-term management of classical maple syrup urine disease

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12 December 2020

Comparison between amino acids and orotic acid analysis in the detection of urea cycle disorders in the Quebec Urinary Screening Program

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12 December 2020

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12 December 2020

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Massachusetts metabolic disorders screening program. I. Technics and results of urine screening

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Ontogeny modifies manifestations of cystinuria genes: implications for counseling

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12 December 2020

Massachusetts Metabolic Disorders Screening Program. II. Methylmalonic aciduria

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12 December 2020

Simple and rapid system for screening and identification of reducing sugars in urine

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12 December 2020

Ontogeny of Amino Acid Reabsorption in Human Kidney. Evidence from the Homozygous Infant with Familial Renal Iminoglycinuria for Multiple Proline and Glycine Systems

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12 December 2020

A cost-benefit analysis of the Quebec Network of Genetic Medicine

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12 December 2020

New disorder of vitamin B12 metabolism (cobalamin F) presenting as methylmalonic aciduria.

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12 December 2020

Urine screening for aminoacidopathies: Is it beneficial?

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Improved direct method for determination of keto acids by 2,4-dinitrophenylhydrazine

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Prolidase deficiency: detection of cases by a newborn urinary screening programme

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12 December 2020

A simple rapid method for the determination of alpha amino acids in urine

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12 December 2020

Urine screening for aminoacidopathies: is it beneficial? Results of a long-term follow-up of cases detected bny screening one millon babies

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12 December 2020

Identifiers

DOI

10.1007/BF01800056

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3128688%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

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