(Q56618727)

4

object named as

Fons J. M. Gabreëls

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author name string

Marjo S. van der Knaap

1

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Ron A. Wevers

2

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Shigeo Kure

3

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Nanda M. Verhoeven

5

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Bertie van Raaij-Selten

6

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Jaak Jaeken

Journal of Child Neurology

7

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publication date

November 1999

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published in

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volume

14

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issue

11

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page(s)

728-731

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cites work

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A new leukoencephalopathy with vanishing white matter.

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Enzymatic diagnosis of nonketotic hyperglycinemia with lymphoblasts

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Glycine modulation of the NMDA receptor/channel complex

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Reference values of neuroactive amino acids in the cerebrospinal fluid by high-performance liquid chromatography with electrochemical and fluorescence detection

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Excitatory amino acids as a final common pathway for neurologic disorders.

21 January 2018

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Neuroexcitatory amino acids and their relation to infarct size and neurological deficit in ischemic stroke

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CSF and serum metabolic profile of patients with Huntington's chorea: a study by high resolution proton NMR spectroscopy and HPLC.

21 January 2018

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A significant reduction of putative transmitter amino acids in cerebrospinal fluid of patients with Parkinson's disease and spinocerebellar degeneration

21 January 2018

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Cerebrospinal fluid analyses in migraine patients and controls

21 January 2018

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Non-ketotic hyperglycinaemia: molecular lesion, diagnosis and pathophysiology

21 January 2018

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Nonketotic hyperglycinemia: analyses of glycine cleavage system in typical and atypical cases

21 January 2018

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Non-ketotic hyperglycinaemia: clinical and biochemical aspects

21 January 2018

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Atypical nonketotic hyperglycinemia confirmed by assay of the glycine cleavage system in lymphoblasts.

21 January 2018

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Nonketotic hyperglycinemia: studies in an atypical variant.

21 January 2018

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Nonketotic hyperglycinemia: Report of a case and review of the clinical, chemical, and pathological changes

21 January 2018

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Glycine Encephalopathy

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The neuropathology of glycine encephalopathy: A report of five cases with immunohistochemical and ultrastructural observations

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Nonketotic hyperglycinemia: atypical clinical and biochemical manifestations

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