O'Rawe A[au] - Search Results

Year	Number of Results
1982	1
1989	1
1990	1
1992	2
1994	1
1995	3
1996	2
1997	5
1998	1
1999	1
2000	2
2006	1
2022	0

1

The Dissociative Experiences Scale.

Lewis CA, Dorahy MJ, O'Rawe B, O'Rawe A. Lewis CA, et al. Among authors: o rawe a. Ir J Psychol Med. 2006 Sep;23(3):121-122. doi: 10.1017/S0790966700009812. Ir J Psychol Med. 2006. PMID: 30290518 No abstract available.

2

Energy metabolism in cystic fibrosis.

O'Rawe A. O'Rawe A. Proc Nutr Soc. 1992 Aug;51(2):237-44. doi: 10.1079/pns19920034. Proc Nutr Soc. 1992. PMID: 1438332 Review. No abstract available.

3

Short stature and malnutrition in cystic fibrosis.

Dodge JA, O'Rawe A. Dodge JA, et al. Among authors: o rawe a. Lancet. 1989 Feb 11;1(8633):331-2. doi: 10.1016/s0140-6736(89)91345-7. Lancet. 1989. PMID: 2563488 No abstract available.

4

Strategy for mutation detection in CLN3: characterisation of two Finnish mutations.

Munroe PB, O'Rawe AM, Mitchison HM, Järvelä IE, Santavuori P, Lerner TJ, Taschner PE, Gardiner RM, Mole SE. Munroe PB, et al. Among authors: o rawe am. Neuropediatrics. 1997 Feb;28(1):15-7. doi: 10.1055/s-2007-973657. Neuropediatrics. 1997. PMID: 9151312

5

Rapid diagnostic test for the major mutation underlying Batten disease.

Järvelä I, Mitchison HM, Munroe PB, O'Rawe AM, Mole SE, Syvänen AC. Järvelä I, et al. Among authors: o rawe am. J Med Genet. 1996 Dec;33(12):1041-2. doi: 10.1136/jmg.33.12.1041. J Med Genet. 1996. PMID: 9004140 Free PMC article.

6

Spectrum of mutations in the Batten disease gene, CLN3.

Munroe PB, Mitchison HM, O'Rawe AM, Anderson JW, Boustany RM, Lerner TJ, Taschner PE, de Vos N, Breuning MH, Gardiner RM, Mole SE. Munroe PB, et al. Among authors: o rawe am. Am J Hum Genet. 1997 Aug;61(2):310-6. doi: 10.1086/514846. Am J Hum Genet. 1997. PMID: 9311735 Free PMC article.

7

Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.

Mitchison HM, Taschner PE, Kremmidiotis G, Callen DF, Doggett NA, Lerner TJ, Janes RB, Wallace BA, Munroe PB, O'Rawe AM, Gardiner RM, Mole SE. Mitchison HM, et al. Among authors: o rawe am. Neuropediatrics. 1997 Feb;28(1):12-4. doi: 10.1055/s-2007-973656. Neuropediatrics. 1997. PMID: 9151311

8

Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic deposits.

O'Rawe A, Mitchison HM, Williams R, Wheeler R, Andermann E, Andermann F, Hart YM, Martin JJ, Philippart M, Stephenson JB, Gardiner RM, Mole SE. O'Rawe A, et al. Neuropediatrics. 1997 Feb;28(1):21-2. doi: 10.1055/s-2007-973659. Neuropediatrics. 1997. PMID: 9151314

9

Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity.

Blouin JL, Meeks M, Radhakrishna U, Sainsbury A, Gehring C, Saïl GD, Bartoloni L, Dombi V, O'Rawe A, Walne A, Chung E, Afzelius BA, Armengot M, Jorissen M, Schidlow DV, van Maldergem L, Walt H, Gardiner RM, Probst D, Guerne PA, Delozier-Blanchet CD, Antonarakis SE. Blouin JL, et al. Among authors: o rawe a. Eur J Hum Genet. 2000 Feb;8(2):109-18. doi: 10.1038/sj.ejhg.5200429. Eur J Hum Genet. 2000. PMID: 10757642

10

A locus for primary ciliary dyskinesia maps to chromosome 19q.

Meeks M, Walne A, Spiden S, Simpson H, Mussaffi-Georgy H, Hamam HD, Fehaid EL, Cheehab M, Al-Dabbagh M, Polak-Charcon S, Blau H, O'Rawe A, Mitchison HM, Gardiner RM, Chung E. Meeks M, et al. Among authors: o rawe a. J Med Genet. 2000 Apr;37(4):241-4. doi: 10.1136/jmg.37.4.241. J Med Genet. 2000. PMID: 10745040 Free PMC article.

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