phenylalanine and ARSA Deficiency

phenylalanine has been researched along with ARSA Deficiency in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Gieselmann, V; Marcão, AM; Miranda, MC; Schindler, K; Schroth, G; Sturzenegger, M; Weis, J; Wiesmann, U; Wiest, R	1
Menkes, JH	1

Other Studies

2 other study(ies) available for phenylalanine and ARSA Deficiency

Article	Year
Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene. Archives of neurology, 2005, Volume: 62, Issue:2 Topics: Adult; Animals; Animals, Newborn; Brain; Cells, Cultured; Cerebroside-Sulfatase; Citric Acid; Cricetinae; DNA Mutational Analysis; Electrophoresis, Gel, Pulsed-Field; Endoplasmic Reticulum; Evoked Potentials; Exons; Female; Gene Expression; Humans; Kidney; Leukodystrophy, Metachromatic; Magnetic Resonance Imaging; Microscopy, Electron, Transmission; Mutagenesis; Mutation; Peripheral Nerves; Phenylalanine; Quaternary Ammonium Compounds; Sural Nerve; Transfection; Valine	2005
Biochemical approaches to the nosology of nervous system defects, III. Birth defects original article series, 1971, Volume: 7, Issue:1 Topics: Ammonia; Biopsy; Brain; Brain Chemistry; Brain Diseases; Cells, Cultured; Chromatography; Fabry Disease; Humans; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lipids; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Spectrometry, Fluorescence	1971

Article

Year

Adult onset metachromatic leukodystrophy without electroclinical peripheral nervous system involvement: a new mutation in the ARSA gene.

Archives of neurology, 2005, Volume: 62, Issue:2

Topics: Adult; Animals; Animals, Newborn; Brain; Cells, Cultured; Cerebroside-Sulfatase; Citric Acid; Cricetinae; DNA Mutational Analysis; Electrophoresis, Gel, Pulsed-Field; Endoplasmic Reticulum; Evoked Potentials; Exons; Female; Gene Expression; Humans; Kidney; Leukodystrophy, Metachromatic; Magnetic Resonance Imaging; Microscopy, Electron, Transmission; Mutagenesis; Mutation; Peripheral Nerves; Phenylalanine; Quaternary Ammonium Compounds; Sural Nerve; Transfection; Valine

2005

Biochemical approaches to the nosology of nervous system defects, III.

Birth defects original article series, 1971, Volume: 7, Issue:1

Topics: Ammonia; Biopsy; Brain; Brain Chemistry; Brain Diseases; Cells, Cultured; Chromatography; Fabry Disease; Humans; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lipids; Metabolism, Inborn Errors; Phenylalanine; Phenylketonurias; Spectrometry, Fluorescence

1971