Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

15 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Long-term neurologic consequences of nutritional vitamin B12 deficiency in infants.
Graham SM, Arvela OM, Wise GA. Graham SM, et al. Among authors: wise ga. J Pediatr. 1992 Nov;121(5 Pt 1):710-4. doi: 10.1016/s0022-3476(05)81897-9. J Pediatr. 1992. PMID: 1432418
The neurological syndrome of infantile cobalamin deficiency: developmental regression and involuntary movements.
Grattan-Smith PJ, Wilcken B, Procopis PG, Wise GA. Grattan-Smith PJ, et al. Among authors: wise ga. Mov Disord. 1997 Jan;12(1):39-46. doi: 10.1002/mds.870120108. Mov Disord. 1997. PMID: 8990052
Smith-Fineman-Myers syndrome in two brothers.
Adès LC, Kerr B, Turner G, Wise G. Adès LC, et al. Am J Med Genet. 1991 Sep 15;40(4):467-70. doi: 10.1002/ajmg.1320400419. Am J Med Genet. 1991. PMID: 1684092
Treatment of infantile phytanic acid storage disease: clinical, biochemical and ultrastructural findings in two children treated for 2 years.
Robertson EF, Poulos A, Sharp P, Manson J, Wise G, Jaunzems A, Carter R. Robertson EF, et al. Eur J Pediatr. 1988 Feb;147(2):133-42. doi: 10.1007/BF00442210. Eur J Pediatr. 1988. PMID: 2452736
Chronic axonal neuropathy with triosephosphate isomerase deficiency.
Wilmshurst JM, Wise GA, Pollard JD, Ouvrier RA. Wilmshurst JM, et al. Among authors: wise ga. Pediatr Neurol. 2004 Feb;30(2):146-8. doi: 10.1016/S0887-8994(03)00423-5. Pediatr Neurol. 2004. PMID: 14984912
Painful torticollis with tongue atrophy--a different neck-tongue syndrome.
O'Meara M, Wise G. O'Meara M, et al. Neuropediatrics. 1995 Oct;26(5):276-80. doi: 10.1055/s-2007-979773. Neuropediatrics. 1995. PMID: 8552222
Hereditary sensory neuropathy type II without trophic changes.
Bye AM, Baker WD, Pollard J, Wise G. Bye AM, et al. Dev Med Child Neurol. 1990 Feb;32(2):164-71. doi: 10.1111/j.1469-8749.1990.tb16915.x. Dev Med Child Neurol. 1990. PMID: 2338180
Hypertrichosis "cubiti" with facial asymmetry.
Edwards MJ, Crawford AE, Jammu V, Wise G. Edwards MJ, et al. Am J Med Genet. 1994 Oct 15;53(1):56-8. doi: 10.1002/ajmg.1320530112. Am J Med Genet. 1994. PMID: 7802037
Phytanic acid oxidase deficiency in childhood.
Wise GA, Duffy BJ, Mitchell JD, Pollard AC, Poulos A, Pollard J. Wise GA, et al. Clin Exp Neurol. 1985;21:289-99. Clin Exp Neurol. 1985. PMID: 3843227
Hereditary motor and sensory neuropathy of neuronal type with onset in early childhood.
Ouvrier RA, McLeod JG, Morgan GJ, Wise GA, Conchin TE. Ouvrier RA, et al. Among authors: wise ga. J Neurol Sci. 1981 Aug;51(2):181-97. doi: 10.1016/0022-510x(81)90097-6. J Neurol Sci. 1981. PMID: 6268756
15 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page
Feedback