Acidemia isovalerica (Italian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acidemia isovalerica" in Italian language version.

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(EN) Y.W. Lee et al., Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia, in Molecular Genetics and Metabolism, vol. 92, 1–2, settembre 2007, pp. 71–77, DOI:10.1016/j.ymgme.2007.05.003, PMID 17576084.
(EN) C. Dionisi-Vici et al., Classical organic acidurias, propionic aciduria, methylmalonic aciduria, and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry, in Journal of Inheritable Metabolic Disorders, vol. 29, 2–3, 2006, pp. 383–389, DOI:10.1007/s10545-006-0278-z, PMID 16763906.
(EN) Sarah Grünert et al., Clinical and neurocognitive outcome in symptomatic isovaleric acidemia, in Orphanet Journal of Rare Diseases, vol. 7, 1º gennaio 2012, p. 9, DOI:10.1186/1750-1172-7-9, ISSN 1750-1172 (WC · ACNP), PMID 22277694.

nestlehealthscience.nl

(FR) Acidémie isovalérique (IVA) | Vitaflo Belgique, su www.nestlehealthscience.nl. URL consultato il 22 febbraio 2022.

nih.gov

ncbi.nlm.nih.gov

(EN) Y.W. Lee et al., Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia, in Molecular Genetics and Metabolism, vol. 92, 1–2, settembre 2007, pp. 71–77, DOI:10.1016/j.ymgme.2007.05.003, PMID 17576084.
(EN) C. Dionisi-Vici et al., Classical organic acidurias, propionic aciduria, methylmalonic aciduria, and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry, in Journal of Inheritable Metabolic Disorders, vol. 29, 2–3, 2006, pp. 383–389, DOI:10.1007/s10545-006-0278-z, PMID 16763906.
(EN) Isovaleric acidemia. Clinical presentation of 6 cases, in The Turkish Journal of Pediatrics, vol. 40, n. 1, 1998, pp. 111–119, PMID 9673537.
(EN) Sarah Grünert et al., Clinical and neurocognitive outcome in symptomatic isovaleric acidemia, in Orphanet Journal of Rare Diseases, vol. 7, 1º gennaio 2012, p. 9, DOI:10.1186/1750-1172-7-9, ISSN 1750-1172 (WC · ACNP), PMID 22277694.

ghr.nlm.nih.gov

(EN) Isovaleric acidemia, in Genetics Home Reference, 4 maggio 2015.

oadoi.org

(EN) Y.W. Lee et al., Different spectrum of mutations of isovaleryl-CoA dehydrogenase (IVD) gene in Korean patients with isovaleric acidemia, in Molecular Genetics and Metabolism, vol. 92, 1–2, settembre 2007, pp. 71–77, DOI:10.1016/j.ymgme.2007.05.003, PMID 17576084.
(EN) C. Dionisi-Vici et al., Classical organic acidurias, propionic aciduria, methylmalonic aciduria, and isovaleric aciduria: long-term outcome and effects of expanded newborn screening using tandem mass spectrometry, in Journal of Inheritable Metabolic Disorders, vol. 29, 2–3, 2006, pp. 383–389, DOI:10.1007/s10545-006-0278-z, PMID 16763906.
(EN) Sarah Grünert et al., Clinical and neurocognitive outcome in symptomatic isovaleric acidemia, in Orphanet Journal of Rare Diseases, vol. 7, 1º gennaio 2012, p. 9, DOI:10.1186/1750-1172-7-9, ISSN 1750-1172 (WC · ACNP), PMID 22277694.

rarediseases.org

(EN) Isovaleric Acidemia, su National Organization for Rare Disorders. URL consultato il 26 febbraio 2023.

unibo.it

acnpsearch.unibo.it

(EN) Sarah Grünert et al., Clinical and neurocognitive outcome in symptomatic isovaleric acidemia, in Orphanet Journal of Rare Diseases, vol. 7, 1º gennaio 2012, p. 9, DOI:10.1186/1750-1172-7-9, ISSN 1750-1172 (WC · ACNP), PMID 22277694.

web.archive.org

(EN) The Online Metabolic and Molecular Bases of Inherited Disease: Home, su ommbid.com. URL consultato il 26 febbraio 2023 (archiviato dall'url originale il 9 dicembre 2008).
(EN) Genova Diagnostics (GDX) - Diagnostic Laboratory Testing for Wellness & Preventive Medicine, su metametrix.com. URL consultato il 26 febbraio 2023 (archiviato dall'url originale il 19 ottobre 2013).

worldcat.org

(EN) Sarah Grünert et al., Clinical and neurocognitive outcome in symptomatic isovaleric acidemia, in Orphanet Journal of Rare Diseases, vol. 7, 1º gennaio 2012, p. 9, DOI:10.1186/1750-1172-7-9, ISSN 1750-1172 (WC · ACNP), PMID 22277694.