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La ricerca find articoli where authors phrase all words ' Rittey, C' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 9 riferimenti
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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
    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
    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
    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
    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
    6. Griffiths, PD; Gardner, SA; Smith, M; Rittey, C; Powell, T
      Hemimegalencephaly and focal megalencephaly in tuberous sclerosis complex

      AMERICAN JOURNAL OF NEURORADIOLOGY
    7. Martland, T; Mbamali, AC; Rittey, C; Tanner, S; Bonham, JR; Griffiths, PD
      Ornithine transcarbamylase deficiency: A case report

      NEUROPEDIATRICS
    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
    9. MARTLAND T; BAXTER P; RITTEY C
      IS THERE AN AGREED TREATMENT FOR CHILDREN IN STATUS EPILEPTICUS

      Developmental Medicine and Child Neurology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 27/01/21 alle ore 22:13:02