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15 results
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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
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