3
- 3-hydroxymethylglutaryl-CoA (3-HMG CoA) Lyase Deficiency
- 3-Methylchrotonyl-CoA (3-MCC) Dehydrogenase Deficiency
A
- A to Z Index
- About Us
- Acute Illness Protocols
- Amino Acid Disorders
- Annual Consortium Meeting
- Annual Meeting Agenda - 2009
- Annual Meeting Summary - 2009
- Arginase Deficiency
- Argininosuccinic Acid Lyase Deficiency (ASA)
- Argininosuccinic Acid Synthetase Deficiency (Citrullinemia) (AS)
B
- Biotinidase Deficiency
C
- Carbamyl Phosphate Synthetase Deficiency (CPS)
- Contact
- CPT I Deficiency
- CPT II Deficiency
D
- Deficiencia de la Deshidrogenasa del Acil-CoA de Cadena Corta (SCADD)
- Discovery of Phenylketonuria (PKU) by Dr. Asbjørn Følling
- Discovery of the Diet for PKU by Dr. Horst Bickel
F
- Family Weekends
- Fatty Acid Oxidation Disorders
- Fatty Acid Oxidation Disorders
- For Families
- For Parents of Babies with Metabolic Disorders
- For Professionals
- For Women with Galactosemia and POI - Your Guide to Taking Action
G
- Galactosemia
- Galactosemia
- Galactosemia: A Guide for Parents of Babies Recently Screened
- Galactosemia: Educators' Resources
- Galactosemia: Resources for Educators
- Guide to Galactosemia and Primary Ovarian Insufficiency (POI)
H
- Health Care Resources
- Health Readiness Assessment
- Home
- Homocystinuria
- Homocystinuria
I
- Infant/Child with Hyperammonemia
- International Conference for Adults and Teens
- Introducing the Newborn Screening Test by Dr. Robert Guthrie
- Isovaleric Acidemia
- IVA
J
- Just for Parents - Your Guide to Talking to Your Daughter About Galactosemia and POI
L
- LCHADD
- Long Chain Hydroxy Acyl-CoA Dehydrogenase Deficiency ( LCHADD)
M
- Maple Syrup Urine Disease (MSUD)
- Maternal PKU Research Study
- MCADD
- Medical Health Summary
- Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)
- Membership
- Metabolic Condition Basics
- Methylmalonic Acidemia
- MSUD
N
- Neonate with Hyperammonemia
- Newborn Screening Guide
- Newborn Screening Guide for Prenatal Educators
- Newborn Screening Prenatal Curriculum
- Newborn Screening Protocols
- News
O
- Organic Acid Disorders
- Organic Acid Disorders
- Ornithine Transcarbamylase (OTC) Deficiency
- Ornithine Transcarbamylase Deficiency (OTC)
- Other Metabolic Disorders
- Other Resources for Families and Women with Galactosemia and POI
P
- PA and MMA
- Phenylketonuria
- Phenylketonuria (PKU)
- Photos!
- PKU Primer for Adolescents and Adults
- PKU: A Guide for Parents of Babies Recently Screened
- Prenatal Education Resources
- Printed Booklets
- Privacy Policy
- Private Test Page
- Propionic Acidemia
- Psychologists' Resources
R
- Regional Metabolic Centers
S
- SCADD
- Short Chain Acyl-CoA Dehydrogenase Deficiency (SCADD)
T
- Talks and Slideshows
- Teachers' Resources
- Teen Challenge
- Terms of Use
- The History of Newborn Screening
- Transition Plan
- Transition to Adult Care
- Transition Toolkit
U
- Understanding Galactosemia
- Urea Cycle Disorders
V
- Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD)
- Video Library
- VLCADD
W
- What to Bring
- Words to Know - A POI Glossary
- Write-Ups & Photos from Past Consortium Meetings
A to Z Index Previous Contact For Families Next
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