Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 148 for acta
Did you mean fact?
  1. Nonbullous congenital ichthyosiform erythroderma 
    ... CASP14 in Patients with Autosomal Recessive Inherited Ichthyosis. Acta Derm Venereol. 2017 Jan 4;97(1):102- ... The role of lipoxygenases in epidermis. Biochim Biophys Acta. 2014 Mar;1841(3):390-400. doi: 10. ...
    https://medlineplus.gov/...ous-congenital-ichthyosiform-erythroderma - Genetics
  2. Actin-accumulation myopathy 
    ... H. Fatal congenital myopathy with actin filament deposits. Acta Neuropathol. 1996 Jul;92(1):104-8. doi: ... muscle alpha-actin diseases (actinopathies): pathology and mechanisms. Acta Neuropathol. 2013 Jan;125(1):19-32. doi: ...
    https://medlineplus.gov/.../condition/actin-accumulation-myopathy - Genetics
  3. CLN4 disease 
    ... has PPT1 pathology and exhibit aberrant protein palmitoylation. Acta Neuropathol. 2016 Apr;131(4):621-37. doi: ... of neuronal ceroid lipofuscinosis-related proteins. Biochim Biophys Acta. 2013 Nov;1832(11):1866-81. doi: 10. ...
    https://medlineplus.gov/genetics/condition/cln4-disease - Genetics
  4. Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency 
    ... cross-sectional study with long-term follow-up. Acta Ophthalmol. 2008 May;86(3):329-37. doi: ... 01121.x. Epub 2007 Dec 19. Erratum In: Acta Ophthalmol. 2008 Jun;86(4):466. Citation on ...
    https://medlineplus.gov/...-hydroxyacyl-coa-dehydrogenase-deficiency - Genetics
  5. Paramyotonia congenita 
    ... in periodic paralysis: a survey of 66 patients. Acta Myol. 2012 Oct;31(2):126-33. Citation ... on PubMed Central Finsterer J. Primary periodic paralyses. Acta Neurol Scand. 2008 Mar;117(3):145-58. ...
    https://medlineplus.gov/genetics/condition/paramyotonia-congenita - Genetics
  6. Hereditary cerebral amyloid angiopathy 
    ... pathogenesis of sporadic and hereditary cerebral amyloid angiopathies. Acta Neuropathol. 2009 Jul;118(1):115-30. doi: ... 0501-8. Epub 2009 Feb 19. Erratum In: Acta Neuropathol. 2009 Aug;118(2):321. Citation on ...
    https://medlineplus.gov/.../hereditary-cerebral-amyloid-angiopathy - Genetics
  7. Triosephosphate isomerase deficiency 
    ... two monomers of the homodimeric enzyme. Biochim Biophys Acta. 2013 Dec;1834(12):2702-11. doi: 10. ... new insights into an enigmatic disease. Biochim Biophys Acta. 2009 Dec;1792(12):1168-74. doi: 10. ...
    https://medlineplus.gov/.../triosephosphate-isomerase-deficiency - Genetics
  8. Mitochondrial complex V deficiency 
    ... have learned by studying its defects. Biochim Biophys Acta. 2009 Jan;1793(1):200-11. doi: 10. ... and genetic defects of ATP synthase. Biochim Biophys Acta. 2006 Sep-Oct;1757(9-10):1400-5. ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  9. CLN3 disease 
    ... of neuronal ceroid lipofuscinosis-related proteins. Biochim Biophys Acta. 2013 Nov;1832(11):1866-81. doi: 10. ... Williams R. NCL diseases - clinical perspectives. Biochim Biophys Acta. 2013 Nov;1832(11):1801-6. doi: 10. ...
    https://medlineplus.gov/genetics/condition/cln3-disease - Genetics
  10. Dihydropyrimidinase deficiency 
    ... structure, reaction mechanisms and enzyme deficiency. Biochim Biophys Acta. 2008 Mar;1784(3):431-44. doi: 10. ... and structural consequences in 17 patients. Biochim Biophys Acta. 2010 Jul-Aug;1802(7-8):639-48. ...
    https://medlineplus.gov/.../condition/dihydropyrimidinase-deficiency - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next