37例酪氨酸血症婴儿的病例经验。 - Suppr

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Experience with 37 infants with tyrosinemia.

作者信息

Larochelle J, Mortezai A, Belanger M, Tremblay M, Claveau J C, Aubin G

出版信息

Can Med Assoc J. 1967 Oct 28;97(18):1051-4.

PMID:6050904

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1923562/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87ae/1923562/da909c5713a7/canmedaj01239-0012-a.jpg

相似文献

Experience with 37 infants with tyrosinemia.

Can Med Assoc J. 1967 Oct 28;97(18):1051-4.

[Disorders in the tyrosine metabolism. II. Tyrosinemia - a congenital metabolic disorder].

Srp Arh Celok Lek. 1974 Jan;102(1):9-20.

[Tyrosinemia].

Cesk Pediatr. 1970 Mar;25(3):109-11.

[Hereditary tyrosinemia].

Union Med Can. 1970 Jun;99(6):1078-82.

[Neonatal transitory tyrosinemia and other types of tyrosinemia].

Minerva Pediatr. 1976 Mar 31;28(11):637-43.

The management of transient tyrosinemia of the newborn.

Pediatrics. 1967 Aug;40(2):308-9.

Genetic aspects of tyrosinemia.

Can Med Assoc J. 1967 Oct 28;97(18):1098-9.

Transient tyrosinemia of the newborn: dietary and clinical aspects.

Pediatrics. 1967 Mar;39(3):378-84.

A patient with tyrosinemia and hypermethioninemia.

Can Med Assoc J. 1967 Oct 28;97(18):1059-67.

[Transient tyrosinemia in a premature infant].

Ugeskr Laeger. 1980 May 12;142(20):1286-7.

引用本文的文献

Physical Growth of Patients with Hereditary Tyrosinaemia Type I: A Single-Centre Retrospective Study.

Nutrients. 2021 Aug 31;13(9):3070. doi: 10.3390/nu13093070.

Type 1 tyrosinemia in Finland: a nationwide study.

Orphanet J Rare Dis. 2020 Oct 12;15(1):281. doi: 10.1186/s13023-020-01547-w.

Hepatorenal tyrosinemia.

Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(5):192-200. doi: 10.2183/pjab.88.192.

Imaging features of type 1 hereditary tyrosinemia: a review of 30 patients.

Pediatr Radiol. 1996 Dec;26(12):845-51. doi: 10.1007/BF03178035.

Screening for tyrosinaemia type I.

Arch Dis Child Fetal Neonatal Ed. 1996 May;74(3):F191-4. doi: 10.1136/fn.74.3.f191.

Acute hepatic failure in children.

Yale J Biol Med. 1984 Mar-Apr;57(2):161-84.

Isovaleric acidemia.

Can Med Assoc J. 1967 Nov 11;97(20):1230-1.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

Hereditary tyrosinemia in a French Canadian isolate.

Am J Hum Genet. 1969 Jan;21(1):36-45.

Disorders of tyrosine metabolism.

Br Med J. 1968 Aug 31;3(5617):511-2.

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相似文献

Experience with 37 infants with tyrosinemia.

Can Med Assoc J. 1967 Oct 28;97(18):1051-4.

[Disorders in the tyrosine metabolism. II. Tyrosinemia - a congenital metabolic disorder].

Srp Arh Celok Lek. 1974 Jan;102(1):9-20.

[Tyrosinemia].

Cesk Pediatr. 1970 Mar;25(3):109-11.

[Hereditary tyrosinemia].

Union Med Can. 1970 Jun;99(6):1078-82.

[Neonatal transitory tyrosinemia and other types of tyrosinemia].

Minerva Pediatr. 1976 Mar 31;28(11):637-43.

The management of transient tyrosinemia of the newborn.

Pediatrics. 1967 Aug;40(2):308-9.

Genetic aspects of tyrosinemia.

Can Med Assoc J. 1967 Oct 28;97(18):1098-9.

Transient tyrosinemia of the newborn: dietary and clinical aspects.

Pediatrics. 1967 Mar;39(3):378-84.

A patient with tyrosinemia and hypermethioninemia.

Can Med Assoc J. 1967 Oct 28;97(18):1059-67.

[Transient tyrosinemia in a premature infant].

Ugeskr Laeger. 1980 May 12;142(20):1286-7.

引用本文的文献

Physical Growth of Patients with Hereditary Tyrosinaemia Type I: A Single-Centre Retrospective Study.

Nutrients. 2021 Aug 31;13(9):3070. doi: 10.3390/nu13093070.

Type 1 tyrosinemia in Finland: a nationwide study.

Orphanet J Rare Dis. 2020 Oct 12;15(1):281. doi: 10.1186/s13023-020-01547-w.

Hepatorenal tyrosinemia.

Proc Jpn Acad Ser B Phys Biol Sci. 2012;88(5):192-200. doi: 10.2183/pjab.88.192.

Imaging features of type 1 hereditary tyrosinemia: a review of 30 patients.

Pediatr Radiol. 1996 Dec;26(12):845-51. doi: 10.1007/BF03178035.

Screening for tyrosinaemia type I.

Arch Dis Child Fetal Neonatal Ed. 1996 May;74(3):F191-4. doi: 10.1136/fn.74.3.f191.

Acute hepatic failure in children.

Yale J Biol Med. 1984 Mar-Apr;57(2):161-84.

Isovaleric acidemia.

Can Med Assoc J. 1967 Nov 11;97(20):1230-1.

Recovery after dietary treatment of an infant with features of tyrosinosis.

Arch Dis Child. 1969 Apr;44(234):258-67. doi: 10.1136/adc.44.234.258.

Hereditary tyrosinemia in a French Canadian isolate.

Am J Hum Genet. 1969 Jan;21(1):36-45.

Disorders of tyrosine metabolism.

Br Med J. 1968 Aug 31;3(5617):511-2.