MacMillan J - Search Results

1

Familial occurrence of idiopathic infantile hypercalcemia.

McTaggart SJ, Craig J, MacMillan J, Burke JR. McTaggart SJ, et al. Among authors: macmillan j. Pediatr Nephrol. 1999 Oct;13(8):668-71. doi: 10.1007/s004670050678. Pediatr Nephrol. 1999. PMID: 10502124

2

Arteriohepatic dysplasia (Alagille syndrome; Watson-Alagille syndrome).

MacMillan JC, Shepherd R, Heritage M. MacMillan JC, et al. Baillieres Clin Gastroenterol. 1998 Jun;12(2):275-91. doi: 10.1016/s0950-3528(98)90135-x. Baillieres Clin Gastroenterol. 1998. PMID: 9890073 Review.

3

Jagged1 (JAG1) mutation detection in an Australian Alagille syndrome population.

Heritage ML, MacMillan JC, Colliton RP, Genin A, Spinner NB, Anderson GJ. Heritage ML, et al. Among authors: macmillan jc. Hum Mutat. 2000 Nov;16(5):408-16. doi: 10.1002/1098-1004(200011)16:5<408::AID-HUMU5>3.0.CO;2-9. Hum Mutat. 2000. PMID: 11058898

4

DHPLC mutation analysis of Jagged1 (JAG1) reveals six novel mutations in Australian alagille syndrome patients.

Heritage ML, MacMillan JC, Anderson GJ. Heritage ML, et al. Among authors: macmillan jc. Hum Mutat. 2002 Dec;20(6):481. doi: 10.1002/humu.9095. Hum Mutat. 2002. PMID: 12442286

5

CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy): an Australian perspective.

Chuah TL, Tan KM, Flanagan S, Hyland V, Sullivan AA, Henderson R, MacMillan J, Lander C. Chuah TL, et al. Among authors: macmillan j. J Clin Neurosci. 2001 Sep;8(5):404-6. doi: 10.1054/jocn.2000.0848. J Clin Neurosci. 2001. PMID: 11535004

6

Novel bovine lentiviral vectors based on Jembrana disease virus.

Metharom P, Takyar S, Xia HH, Ellem KA, Macmillan J, Shepherd RW, Wilcox GE, Wei MQ. Metharom P, et al. Among authors: macmillan j. J Gene Med. 2000 May-Jun;2(3):176-85. doi: 10.1002/(SICI)1521-2254(200005/06)2:3<176::AID-JGM106>3.0.CO;2-Q. J Gene Med. 2000. PMID: 10894263

7

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees.

Curtain RP, Lea RA, Tajouri L, Haupt LM, Ovcaric M, MacMillan J, Griffiths LR. Curtain RP, et al. Among authors: macmillan j. Neurol Res. 2005 Sep;27(6):647-52. doi: 10.1179/016164105X39978. Neurol Res. 2005. PMID: 16157018

8

Adult onset Krabbe disease may mimic motor neurone disease.

Henderson RD, MacMillan JC, Bradfield JM. Henderson RD, et al. Among authors: macmillan jc. J Clin Neurosci. 2003 Sep;10(5):638-9. doi: 10.1016/s0967-5868(02)00302-8. J Clin Neurosci. 2003. PMID: 12948479

9

Novel mutations in the DYNC1H1 tail domain refine the genetic and clinical spectrum of dyneinopathies.

Peeters K, Bervoets S, Chamova T, Litvinenko I, De Vriendt E, Bichev S, Kancheva D, Mitev V, Kennerson M, Timmerman V, De Jonghe P, Tournev I, MacMillan J, Jordanova A. Peeters K, et al. Among authors: macmillan j. Hum Mutat. 2015 Mar;36(3):287-91. doi: 10.1002/humu.22744. Hum Mutat. 2015. PMID: 25512093

10

Novel mutation of the myelin P0 gene in a CMT1B family.

Sorour E, MacMillan J, Upadhyaya M. Sorour E, et al. Among authors: macmillan j. Hum Mutat. 1997;9(1):74-7. doi: 10.1002/(SICI)1098-1004(1997)9:1<74::AID-HUMU16>3.0.CO;2-M. Hum Mutat. 1997. PMID: 8990016 No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

434 results

Search Page