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1. Wilmshurst, JM; Bye, A; Rittey, C; Adams, C; Hahn, AF; Ramsay, D; Pamphlett, R; Pollard, JD; Ouvrier, R
   Severe infantile axonal neuropathy with respiratory failure
   MUSCLE & NERVE
   
   J.M. Wilmshurst et al., "Severe infantile axonal neuropathy with respiratory failure", MUSCLE NERV, 24(6), 2001, pp. 760-768
2. Crow, YJ; Jackson, AP; Roberts, E; van Beusekom, E; Barth, P; Corry, P; Ferrie, CD; Hamel, BCJ; Jayatunga, R; Karbani, G; Kalmanchey, R; Kelemen, A; King, M; Kumar, R; Livingstone, J; Massey, R; McWilliam, R; Meager, A; Rittey, C; Stephenson, JBP; Tolmie, JL; Verrips, A; Voit, T; van Bokhoven, H; Brunner, HG; Woods, CG
   Aicardi-Goutieres syndrome display genetic heterogeneity with one locus (AGS1) on chromosome 3p21
   AMERICAN JOURNAL OF HUMAN GENETICS
   
   Y.J. Crow et al., "Aicardi-Goutieres syndrome display genetic heterogeneity with one locus (AGS1) on chromosome 3p21", AM J HU GEN, 67(1), 2000, pp. 213-221
3. Bonham, JR; Guthrie, P; Downing, M; Allen, JC; Tanner, MS; Sharrard, M; Rittey, C; Land, JM; Fensom, A; O'Neill, D; Duley, JA; Fairbanks, LD
   The allopurinol load test lacks specificity for primary urea cycle defectsbut may indicate unrecognized mitochondrial disease
   JOURNAL OF INHERITED METABOLIC DISEASE
   
   J.R. Bonham et al., "The allopurinol load test lacks specificity for primary urea cycle defectsbut may indicate unrecognized mitochondrial disease", J INH MET D, 22(2), 1999, pp. 174-184
4. Faure, S; Bordelais, I; Marquette, C; Rittey, C; Campos-Castello, J; Goutieres, F; Ponsot, G; Weissenbach, J; Lebon, P
   Aicardi-Goutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?
   CLINICAL GENETICS
   
   S. Faure et al., "Aicardi-Goutieres syndrome: monogenic recessive disease, genetically heterogeneous disease, or multifactorial disease?", CLIN GENET, 56(2), 1999, pp. 149-153
5. Yanai, S; Baxter, P; Rittey, C; Guthrie, P; Bonham, J; Tanner, S; Heales, S
   Clinical and laboratory findings in referrals for mitochondrial DNA analysis
   ARCHIVES OF DISEASE IN CHILDHOOD
   
   S. Yanai et al., "Clinical and laboratory findings in referrals for mitochondrial DNA analysis", ARCH DIS CH, 81(5), 1999, pp. 460-460
6. Griffiths, PD; Gardner, SA; Smith, M; Rittey, C; Powell, T
   Hemimegalencephaly and focal megalencephaly in tuberous sclerosis complex
   AMERICAN JOURNAL OF NEURORADIOLOGY
   
   P.D. Griffiths et al., "Hemimegalencephaly and focal megalencephaly in tuberous sclerosis complex", AM J NEUROR, 19(10), 1998, pp. 1935-1938
7. Martland, T; Mbamali, AC; Rittey, C; Tanner, S; Bonham, JR; Griffiths, PD
   Ornithine transcarbamylase deficiency: A case report
   NEUROPEDIATRICS
   
   T. Martland et al., "Ornithine transcarbamylase deficiency: A case report", NEUROPEDIAT, 29(6), 1998, pp. 331-332
8. KUMAR D; RITTEY C; CAMERON AH; VARIEND S
   RECOGNIZABLE INHERITED SYNDROME OF PROGRESSIVE CENTRAL-NERVOUS-SYSTEMDEGENERATION AND GENERALIZED INTRACRANIAL CALCIFICATION WITH OVERLAPPING PHENOTYPE OF THE SYNDROME OF AICARDI AND GOUTIERES
   American journal of medical genetics
   
   D. Kumar et al., "RECOGNIZABLE INHERITED SYNDROME OF PROGRESSIVE CENTRAL-NERVOUS-SYSTEMDEGENERATION AND GENERALIZED INTRACRANIAL CALCIFICATION WITH OVERLAPPING PHENOTYPE OF THE SYNDROME OF AICARDI AND GOUTIERES", American journal of medical genetics, 75(5), 1998, pp. 508-515
9. MARTLAND T; BAXTER P; RITTEY C
   IS THERE AN AGREED TREATMENT FOR CHILDREN IN STATUS EPILEPTICUS
   Developmental Medicine and Child Neurology
   
   T. Martland et al., "IS THERE AN AGREED TREATMENT FOR CHILDREN IN STATUS EPILEPTICUS", Developmental Medicine and Child Neurology, 40(4), 1998, pp. 286-287