R Matalon Selected Research

Microcephaly

10/2000	The International Collaborative Study of Maternal Phenylketonuria: status report 1998.
1/2000	Maternal phenylketonuria syndrome: congenital heart defects, microcephaly, and developmental outcomes.

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R Matalon Research Topics

Disease

7	Phenylketonurias (Phenylketonuria) 08/2017 - 01/2000
4	Canavan Disease (Leukodystrophy, Spongiform) 03/2004 - 01/2000
2	Intellectual Disability (Idiocy) 03/2004 - 05/2000
2	Congenital Heart Defects (Congenital Heart Defect) 05/2001 - 01/2000
2	Microcephaly 10/2000 - 01/2000
1	Muscle Hypotonia (Hypotonia) 03/2004
1	Headache (Headaches) 01/2003
1	Nervous System Diseases (Neurological Disorders) 07/2000
1	Congenital Abnormalities (Deformity) 02/2000
1	Maternal Phenylketonuria 02/2000

Drug/Important Bio-Agent (IBA)

6	Phenylalanine (L-Phenylalanine)FDA Link 04/2007 - 01/2000
4	Neutral Amino AcidsIBA 08/2017 - 12/2006
3	aspartoacylaseIBA 07/2000 - 01/2000
2	Phenylalanine Hydroxylase (Phenylalanine 4 Monooxygenase)IBA 01/2017 - 05/2001
2	N-acetylaspartate (N-acetyl aspartate)IBA 03/2004 - 05/2000
1	Succinate-Semialdehyde Dehydrogenase (Succinic Semialdehyde Dehydrogenase)IBA 03/2004
1	Dietary ProteinsIBA 01/2003
1	Proteins (Proteins, Gene)FDA Link 01/2003
1	OF 900IBA 05/2001
1	LipidsIBA 07/2000