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Items: 1 to 20 of 89

1.

E7 (1057ΔTA) mutation of the acidic α-glucosidase gene causes Pompe's disease in Droughtmaster cattle.

Lyons RE, Johnston DJ, McGowan MR, Laing A, Robinson B, Owen H, Hill BD, Burns BM.

Aust Vet J. 2017 May;95(5):138-142. doi: 10.1111/avj.12575.

PMID:
28444756
2.

Genotyping Brahman cattle for generalised glycogenosis.

Dennis JA, Healy PJ, Reichmann KG.

Aust Vet J. 2002 May;80(5):286-91.

PMID:
12074310
3.

Biochemical genetics of glycogenosis type II in Brahman cattle.

Wisselaar HA, Hermans MM, Visser WJ, Kroos MA, Oostra BA, Aspden W, Harrison B, Hetzel DJ, Reuser AJ, Drinkwater RD.

Biochem Biophys Res Commun. 1993 Feb 15;190(3):941-7.

PMID:
8439343
4.

Generalised glycogenosis in Brahman cattle.

O'Sullivan BM, Healy PJ, Fraser IR, Nieper RE, Whittle RJ, Sewell CA.

Aust Vet J. 1981 May;57(5):227-9.

PMID:
6945845
6.

Clinical, diagnostic and biochemical features of generalised glycogenosis type II in Brahman cattle.

Reichmann KG, Twist JO, Thistlethwaite EJ.

Aust Vet J. 1993 Nov;70(11):405-8.

PMID:
8280022
7.

Genotyping shorthorn cattle for generalised glycogenosis.

Dennis JA, Healy PJ.

Aust Vet J. 2001 Nov;79(11):773-5.

PMID:
11789914
8.

Generalized glycogenosis in Brahman-derived breeds: diagnosis and prevalence in Argentina.

Caffaro ME, Raschia MA, Amadio AF, Poli MA.

Trop Anim Health Prod. 2019 Aug 3. doi: 10.1007/s11250-019-02026-6. [Epub ahead of print]

PMID:
31377960
9.

Infantile and late onset form of generalised glycogenosis type II in cattle.

Howell JM, Dorling PR, Cook RD, Robinson WF, Bradley S, Gawthorne JM.

J Pathol. 1981 Aug;134(4):267-77.

PMID:
7033492
10.
11.
12.

Natural bone marrow transplantation in cattle with Pompe's disease.

Howell JM, Dorling PR, Shelton JN, Taylor EG, Palmer DG, Di Marco PN.

Neuromuscul Disord. 1991;1(6):449-54.

PMID:
1822357
13.

Bovine glycogenosis type II: the molecular defect in Shorthorn cattle.

Palmer DG, Dorling PR, Howell JM.

Neuromuscul Disord. 1994 Jan;4(1):39-48.

PMID:
8173350
14.

Evidence of molecular heterogeneity for generalised glycogenosis between and within breeds of cattle.

Healy PJ, Nicholls PJ, Martiniuk F, Tzall S, Hirschhorn R, Howell JM.

Aust Vet J. 1995 Aug;72(8):309-11.

PMID:
8579563
15.
16.

Homozygotic intronic GAA mutation in three siblings with late-onset Pompe's disease.

Grzesiuk AK, Shinjo SM, da Silva R, Machado M, Galera MF, Marie SK.

Arq Neuropsiquiatr. 2010 Apr;68(2):194-7.

17.

Genotyping glycogen storage disease type II and type V in cattle reared in the Czech Republic.

Cítek J, Rehout V, Vecerek L, Hájková J.

J Vet Med A Physiol Pathol Clin Med. 2007 Jun;54(5):257-9.

PMID:
17523960
18.

Haemopoietic chimaerism: a complication in heterozygote detection tests for inherited defects in cattle.

Healy PJ, Dennis JA, Nicholls PJ, Reichmann KG.

Anim Genet. 1994 Feb;25(1):1-6.

PMID:
8161014
19.

Control of generalised glycogenosis in a Brahman herd.

Healy PJ, Sewell CA, Nieper RE, Whittle RJ, Reichmann KG.

Aust Vet J. 1987 Sep;64(9):278-80. No abstract available.

PMID:
3480704
20.

Adult glycogenosis type II (Pompe's disease): morphological abnormalities in muscle and skin biopsies compared with acid alpha-glucosidase activity.

Wierzba-Bobrowicz T, Lewandowska E, Lugowska A, Rola R, Stepień T, Ryglewicz D, Pasennik E.

Folia Neuropathol. 2007;45(4):179-86.

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