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Results 1 - 8 of 8 for Spectroscopy
  1. Aminoacylase 1 deficiency 
    ... J, Hart C, Omran H, Wevers RA. NMR spectroscopy of aminoacylase 1 deficiency, a novel inborn error ...
    https://medlineplus.gov/genetics/condition/aminoacylase-1-deficiency - Genetics
  2. Mucolipidosis II alpha/beta 
    ... H. Hypoyelination in I-cell disease; MRI, MR spectroscopy and neuropathological correlation. Brain Dev. 2012 Oct;34( ...
    https://medlineplus.gov/.../condition/mucolipidosis-ii-alpha-beta - Genetics
  3. GABA-transaminase deficiency 
    ... of GABA transaminase deficiency facilitated by proton MR spectroscopy. J Inherit Metab Dis. 2010 Feb;33(1): ...
    https://medlineplus.gov/.../condition/gaba-transaminase-deficiency - Genetics
  4. Leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation 
    ... is identified using another test called magnetic resonance spectroscopy (MRS). LBSL is a rare condition. Its exact ...
    https://medlineplus.gov/...al-cord-involvement-and-lactate-elevation - Genetics
  5. ABAT gene 
    ... of GABA transaminase deficiency facilitated by proton MR spectroscopy. J Inherit Metab Dis. 2010 Feb;33(1): ...
    https://medlineplus.gov/genetics/gene/abat - Genetics
  6. Adult polyglucosan body disease 
    ... A. Adult polyglucosan body disease: proton magnetic resonance spectroscopy of the brain and novel mutation in the ...
    https://medlineplus.gov/.../adult-polyglucosan-body-disease - Genetics
  7. Canavan disease 
    ... of Canavan disease revealed by proton magnetic resonance spectroscopy (1H-MRS) and diffusion-weighted MRI. Neuropediatrics. 2006 ...
    https://medlineplus.gov/genetics/condition/canavan-disease - Genetics
  8. GBE1 gene 
    ... A. Adult polyglucosan body disease: proton magnetic resonance spectroscopy of the brain and novel mutation in the ...
    https://medlineplus.gov/genetics/gene/gbe1 - Genetics