PubMed (OMIM) for id: 3242

Year	Number of Results
1957	1
1960	1
1975	1
1977	1
1981	1
1983	2
1990	1
1991	1
1992	1
1993	1
1994	1
1995	2
1997	2
1999	1
2000	2
2001	1
2007	1
2016	1
2019	1
2024	0

1

Hawkinsinuria With Direct Hyperbilirubinemia in Egyptian-Lebanese Boy.

El Khatib H, Asaad B, Zaylaa A, Awad F, Sbeity M, Mneimneh S, Haber G, Naja Z, Rajab M. El Khatib H, et al. Front Pediatr. 2019 Mar 29;7:69. doi: 10.3389/fped.2019.00069. eCollection 2019. Front Pediatr. 2019. PMID: 30984715 Free PMC article.

2

Hawkinsinuria in two unrelated Greek newborns: identification of a novel variant, biochemical findings and treatment.

Thodi G, Schulpis KH, Dotsikas Y, Pavlides C, Molou E, Chatzidaki M, Triantafylli O, Loukas YL. Thodi G, et al. J Pediatr Endocrinol Metab. 2016 Jan;29(1):15-20. doi: 10.1515/jpem-2015-0132. J Pediatr Endocrinol Metab. 2016. PMID: 26226126 Free article.

3

Manifestation of hawkinsinuria in a patient compound heterozygous for hawkinsinuria and tyrosinemia III.

Item CB, Mihalek I, Lichtarge O, Jalan A, Vodopiutz J, Muhl A, Bodamer OA. Item CB, et al. Mol Genet Metab. 2007 Aug;91(4):379-83. doi: 10.1016/j.ymgme.2007.04.008. Epub 2007 Jun 7. Mol Genet Metab. 2007. PMID: 17560158

4

An inborn defect in the metabolism of tyrosine in infants on a normal diet.

Bloxam HR, Day MG, Gibbs NK, Woolf LI. Bloxam HR, et al. Biochem J. 1960 Nov;77(2):320-6. doi: 10.1042/bj0770320. Biochem J. 1960. PMID: 16748849 Free PMC article. No abstract available.

5

p-Hydroxyphenylpyruvate oxidase of liver.

HAGER SE, GREGERMAN RI, KNOX WE. HAGER SE, et al. J Biol Chem. 1957 Apr;225(2):935-47. J Biol Chem. 1957. PMID: 13416295 Free article. No abstract available.

6

Outcome of tyrosinaemia type III.

Ellaway CJ, Holme E, Standing S, Preece MA, Green A, Ploechl E, Ugarte M, Trefz FK, Leonard JV. Ellaway CJ, et al. J Inherit Metab Dis. 2001 Dec;24(8):824-32. doi: 10.1023/a:1013936107064. J Inherit Metab Dis. 2001. PMID: 11916315

7

Mutations in the 4-hydroxyphenylpyruvic acid dioxygenase gene are responsible for tyrosinemia type III and hawkinsinuria.

Tomoeda K, Awata H, Matsuura T, Matsuda I, Ploechl E, Milovac T, Boneh A, Scott CR, Danks DM, Endo F. Tomoeda K, et al. Mol Genet Metab. 2000 Nov;71(3):506-10. doi: 10.1006/mgme.2000.3085. Mol Genet Metab. 2000. PMID: 11073718

8

Mutations in the 4-hydroxyphenylpyruvate dioxygenase gene (HPD) in patients with tyrosinemia type III.

Rüetschi U, Cerone R, Pérez-Cerda C, Schiaffino MC, Standing S, Ugarte M, Holme E. Rüetschi U, et al. Hum Genet. 2000 Jun;106(6):654-62. doi: 10.1007/s004390000307. Hum Genet. 2000. PMID: 10942115

9

Long-term follow up of a new case of hawkinsinuria.

Lehnert W, Stögmann W, Engelke U, Wevers RA, van den Berg GB. Lehnert W, et al. Eur J Pediatr. 1999 Jul;158(7):578-82. doi: 10.1007/s004310051151. Eur J Pediatr. 1999. PMID: 10412819

10

Tyrosinemia type III: diagnosis and ten-year follow-up.

Cerone R, Holme E, Schiaffino MC, Caruso U, Maritano L, Romano C. Cerone R, et al. Acta Paediatr. 1997 Sep;86(9):1013-5. doi: 10.1111/j.1651-2227.1997.tb15192.x. Acta Paediatr. 1997. PMID: 9343288

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