Murphey WH[au] - Search Results

Year	Number of Results
1964	3
1967	4
1970	1
1972	1
1973	1
1975	1
1976	1
1977	2
1978	2
1979	3
1989	1
1991	1
1993	2
1994	1
1995	1
1996	1
1997	1
2001	1
2023	0

1

Molecular advances in retinitis pigmentosa.

Weleber RG, Murphey WH. Weleber RG, et al. Among authors: murphey wh. West J Med. 1991 Oct;155(4):423-4. West J Med. 1991. PMID: 1771891 Free PMC article. No abstract available.

2

Maternal phenylketonuria.

Buist NR, Lis EW, Tuerck JM, Murphey WH. Buist NR, et al. Among authors: murphey wh. Lancet. 1979 Sep 15;2(8142):589. doi: 10.1016/s0140-6736(79)91648-9. Lancet. 1979. PMID: 89575 No abstract available.

3

Neonatal screening for alpha1-antitrypsin deficiency.

O'Brien ML, Buist NR, Murphey WH. O'Brien ML, et al. Among authors: murphey wh. J Pediatr. 1978 Jun;92(6):1006-10. doi: 10.1016/s0022-3476(78)80388-6. J Pediatr. 1978. PMID: 307054 No abstract available.

4

MANNITOL CATABOLISM BY STAPHYLOCOCCUS AUREUS.

MURPHEY WH, ROSENBLUM ED. MURPHEY WH, et al. Arch Biochem Biophys. 1964 Aug;107:292-7. doi: 10.1016/0003-9861(64)90332-7. Arch Biochem Biophys. 1964. PMID: 14224835 No abstract available.

5

Serum carnosinase deficiency concomitant with mental retardation.

Murphey WH, Lindmark DG, Patchen LI, Housler ME, Harrod EK, Mosovich L. Murphey WH, et al. Pediatr Res. 1973 Jul;7(7):601-6. doi: 10.1203/00006450-197307000-00001. Pediatr Res. 1973. PMID: 4718759 No abstract available.

6

Ophthalmologic screening of deaf students in Oregon.

Brinks MV, Murphey WH, Cardwell W, Otos M, Weleber RG. Brinks MV, et al. Among authors: murphey wh. J Pediatr Ophthalmol Strabismus. 2001 Jan-Feb;38(1):11-5. doi: 10.3928/0191-3913-20010101-06. J Pediatr Ophthalmol Strabismus. 2001. PMID: 11201911

7

Neonatal hypothyroidism detected by the Northwest Regional Screening Program.

LaFranchi SH, Murphey WH, Foley TP Jr, Larsen PR, Buist NR. LaFranchi SH, et al. Among authors: murphey wh. Pediatrics. 1979 Feb;63(2):180-91. Pediatrics. 1979. PMID: 108659

8

Obstructive airway disease associated with heterozygous alpha-1-antitrypsin deficiency.

Johnson TF, Reisman RE, Arbesman CE, Mattar AG, Murphey WH. Johnson TF, et al. Among authors: murphey wh. J Allergy Clin Immunol. 1976 Jul;58(1 PT 1):69-75. doi: 10.1016/0091-6749(76)90108-1. J Allergy Clin Immunol. 1976. PMID: 1084893

9

Dystrophin expression in the human retina is required for normal function as defined by electroretinography.

Pillers DA, Bulman DE, Weleber RG, Sigesmund DA, Musarella MA, Powell BR, Murphey WH, Westall C, Panton C, Becker LE, et al. Pillers DA, et al. Among authors: murphey wh. Nat Genet. 1993 May;4(1):82-6. doi: 10.1038/ng0593-82. Nat Genet. 1993. PMID: 8513332

10

A heterozygous putative null mutation in ROM1 without a mutation in peripherin/RDS in a family with retinitis pigmentosa.

Sakuma H, Inana G, Murakami A, Yajima T, Weleber RG, Murphey WH, Gass JD, Hotta Y, Hayakawa M, Fujiki K, et al. Sakuma H, et al. Among authors: murphey wh. Genomics. 1995 May 20;27(2):384-6. doi: 10.1006/geno.1995.1066. Genomics. 1995. PMID: 7558016 Free article. No abstract available.

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