<--- Back to Details
First PageDocument Content
Medicine / Rare diseases / Guanidines / Amino acids / Nitrogen metabolism / Argininosuccinate synthase / Newborn screening / Citrulline / Argininosuccinic aciduria / Urea cycle / Chemistry / Health
Medicine
Rare diseases
Guanidines
Amino acids
Nitrogen metabolism
Argininosuccinate synthase
Newborn screening
Citrulline
Argininosuccinic aciduria
Urea cycle
Chemistry
Health

Visio-Citrulline[removed] no edits.vsd

Add to Reading List

Source URL: www.ncbi.nlm.nih.gov

Download Document from Source Website

File Size: 106,46 KB

Share Document on Facebook

Similar Documents

Newborn screening / Isovaleric acidemia / Galactosemia / Methylmalonic acidemia / Propionic acidemia / Malonyl-CoA decarboxylase deficiency / Inborn error of metabolism / Argininosuccinic aciduria / Organic acidemia / Health / Rare diseases / Medicine

TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD

DocID: 12v8A - View Document

Anatomy / Thyroid disease / Pediatrics / Rare diseases / Epidemiology / Newborn screening / Congenital hypothyroidism / Argininosuccinic aciduria / Urea cycle disorder / Health / Biology / Urea cycle

Volume 6, Issue 1 April 2011 State of Tennessee Department of Health

DocID: Jss2 - View Document

Health / Urea cycle disorder / Ornithine transcarbamylase deficiency / Argininosuccinic aciduria / Hyperammonemia / Ornithine translocase deficiency / Arginase / Citrullinemia / N-Acetylglutamate synthase deficiency / Urea cycle / Metabolism / Biology

UCDC Newsletter_4.22.13_Final.pub

DocID: HWNL - View Document

Anatomy / Thyroid disease / Pediatrics / Rare diseases / Epidemiology / Newborn screening / Congenital hypothyroidism / Argininosuccinic aciduria / Urea cycle disorder / Health / Biology / Urea cycle

Volume 6, Issue 1 April 2011 State of Tennessee Department of Health

DocID: Heit - View Document

Argininosuccinic aciduria / Hyperammonemia / Organic acidemia / Carnitine / Medical genetics / Medicine / Health / Rare diseases

Diagnosis: Argininosuccinic Aciduria or Arginosuccinic Lyase Deficiency (ASA) ASA is an inherited disorder that limits the body’s ability to convert ammonia to urea. During periods of illness, fasting or protein overlo

DocID: BM9n - View Document