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Results: 1-25 | 26-34
Results: 1-25/34
Carbonic anhydrase localization in charophycean green algae: Ecological and evolutionary significance
Authors: Arancibia-Avila, P Coleman, JR Russin, WA Graham, JM Graham, LE
Citation: P. Arancibia-avila et al., Carbonic anhydrase localization in charophycean green algae: Ecological and evolutionary significance, INT J PL SC, 162(1), 2001, pp. 127-135
Cross-modal plasticity underpins language recovery after cochlear implantation
Authors: Giraud, AL Price, CJ Graham, JM Truy, E Frackowiak, RSJ
Citation: Al. Giraud et al., Cross-modal plasticity underpins language recovery after cochlear implantation, NEURON, 30(3), 2001, pp. 657-663
Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations
Authors: Rosenberg, MJ Killoran, C Dziadzio, L Chang, S Stone, DL Meck, J Aughton, D Bird, LM Bodurtha, J Cassidy, SB Graham, JM Grix, A Guttmacher, AE Hudgins, L Kozma, C Michaelis, RC Pauli, R Peters, KF Rosenbaum, KN Tifft, CJ Wargowski, D Williams, MS Biesecker, LG
Citation: Mj. Rosenberg et al., Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations, HUM GENET, 109(3), 2001, pp. 311-318
Radiographic findings and Gs-alpha bioactivity studies and mutation screening in acrodysostosis indicate a different etiology from pseudohypoparathyroidism
Authors: Graham, JM Krakow, D Tolo, VT Smith, AK Lachman, RS
Citation: Jm. Graham et al., Radiographic findings and Gs-alpha bioactivity studies and mutation screening in acrodysostosis indicate a different etiology from pseudohypoparathyroidism, PEDIAT RAD, 31(1), 2001, pp. 2-9
Is there a functioning vestibulocochlear nerve? Cochlear implantation in achild with symmetrical auditory findings but asymmetric imaging
Authors: Acker, T Mathur, NN Savy, L Graham, JM
Citation: T. Acker et al., Is there a functioning vestibulocochlear nerve? Cochlear implantation in achild with symmetrical auditory findings but asymmetric imaging, INT J PED O, 57(2), 2001, pp. 171-176
Editorial comment - A recognizable syndrome within CHARGE association: Hall-Hittner syndrome
Authors: Graham, JM
Citation: Jm. Graham, Editorial comment - A recognizable syndrome within CHARGE association: Hall-Hittner syndrome, AM J MED G, 99(2), 2001, pp. 120-123
Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3
Authors: Schweitzer, DN Graham, JM Lachman, RS Jabs, EW Okajima, K Przylepa, KA Shanske, A Chen, K Neidich, JA Wilcox, WR
Citation: Dn. Schweitzer et al., Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3, AM J MED G, 98(1), 2001, pp. 75-91
Syndromic ear anomalies and renal ultrasounds
Authors: Wang, RY Earl, DL Ruder, RO Graham, JM
Citation: Ry. Wang et al., Syndromic ear anomalies and renal ultrasounds, PEDIATRICS, 108(2), 2001, pp. NIL_74-NIL_81
Statistics with confidence.
Authors: Graham, JM
Citation: Jm. Graham, Statistics with confidence., EDUC PSYC M, 61(4), 2001, pp. 668-674
Functional plasticity of language-related brain areas after cochlear implantation
Authors: Giraud, AL Price, CJ Graham, JM Frackowiak, RSJ
Citation: Al. Giraud et al., Functional plasticity of language-related brain areas after cochlear implantation, BRAIN, 124, 2001, pp. 1307-1316
Brain iron deposition in Parkinson's disease imaged using the PRIME magnetic resonance sequence (vol 123, pg 2423, 2000)
Authors: Graham, JM Paley, MNJ Grunewald, RA Hoggard, N Griffiths, PD
Citation: Jm. Graham et al., Brain iron deposition in Parkinson's disease imaged using the PRIME magnetic resonance sequence (vol 123, pg 2423, 2000), BRAIN, 124, 2001, pp. 1258-1258
Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy
Authors: Graham, JM Anyane-Yeboa, K Raams, A Appeldoorn, E Kleijer, WJ Garritsen, VH Busch, D Edersheim, TG Jaspers, NGJ
Citation: Jm. Graham et al., Cerebro-oculo-facio-skeletal syndrome with a nucleotide excision-repair defect and a mutated XPD gene, with prenatal diagnosis in a triplet pregnancy, AM J HU GEN, 69(2), 2001, pp. 291-300
Separation of plasma lipoproteins in self-generated gradients of iodixanol
Authors: Higgins, JA Graham, JM Davies, IG
Citation: Ja. Higgins et al., Separation of plasma lipoproteins in self-generated gradients of iodixanol, METH MOL M, 52, 2001, pp. 37-49
Fractionation of lipoprotein subclasses in self-generated gradients of iodixanol
Authors: Graham, JM Griffin, BA Davies, IG Higgins, JA
Citation: Jm. Graham et al., Fractionation of lipoprotein subclasses in self-generated gradients of iodixanol, METH MOL M, 52, 2001, pp. 51-59
Association study of dopamine receptor gene polymorphisms with drug-induced hallucinations in patients with idiopathic Parkinson's disease
Authors: Makoff, AJ Graham, JM Arranz, MJ Forsyth, J Li, T Aitchison, KJ Shaikh, S Grunewald, RA
Citation: Aj. Makoff et al., Association study of dopamine receptor gene polymorphisms with drug-induced hallucinations in patients with idiopathic Parkinson's disease, PHARMACOGEN, 10(1), 2000, pp. 43-48
Blaschkolinear skin pigmentary variation due to trisomy 7 mosaicism
Authors: Kayser, M Henderson, LB Kreutzman, J Schreck, R Graham, JM
Citation: M. Kayser et al., Blaschkolinear skin pigmentary variation due to trisomy 7 mosaicism, AM J MED G, 95(3), 2000, pp. 281-284
Cole-Hughes macrocephaly syndrome and associated autistic manifestations
Authors: Naqvi, S Cole, T Graham, JM
Citation: S. Naqvi et al., Cole-Hughes macrocephaly syndrome and associated autistic manifestations, AM J MED G, 94(2), 2000, pp. 149-152
Teratology society public affairs committee position paper: Thalidomide
Authors: Adams, J Buttar, HS Chambers, C Collins, TFX Graham, JM Jones, KL Kweder, S Mitala, J Polifka, JE Schwetz, BA
Citation: J. Adams et al., Teratology society public affairs committee position paper: Thalidomide, TERATOLOGY, 62(3), 2000, pp. 172-173
DIC-mediated coupling of carboxylic acids to (4R, 5S)-4-methyl-5-phenyl-2-oxazolidinone
Authors: Graham, JM Shireman, BT Maddux, TM Brandstedt, CM Zeller, WE
Citation: Jm. Graham et al., DIC-mediated coupling of carboxylic acids to (4R, 5S)-4-methyl-5-phenyl-2-oxazolidinone, SYN COMMUN, 30(7), 2000, pp. 1221-1226
Congenital malformations of the ear and cochlear implantation in children:review and temporal bone report of common cavity
Authors: Graham, JM Phelps, PD Michaels, L
Citation: Jm. Graham et al., Congenital malformations of the ear and cochlear implantation in children:review and temporal bone report of common cavity, J LARYNG OT, 114, 2000, pp. 1-14
Effects of pH on cell morphology and carbonic anhydrase activity and localization in bloom-forming Mougeotia (Chlorophyta, Charophyceae)
Authors: Arancibia-Avila, P Coleman, JR Russin, WA Wilcox, LW Graham, JM Graham, LE
Citation: P. Arancibia-avila et al., Effects of pH on cell morphology and carbonic anhydrase activity and localization in bloom-forming Mougeotia (Chlorophyta, Charophyceae), CAN J BOTAN, 78(9), 2000, pp. 1206-1214
Brain iron deposition in Parkinson's disease imaged using the PRIME magnetic resonance sequence
Authors: Graham, JM Paley, MNJ Grunewald, RA Hoggard, N Griffiths, PD
Citation: Jm. Graham et al., Brain iron deposition in Parkinson's disease imaged using the PRIME magnetic resonance sequence, BRAIN, 123, 2000, pp. 2423-2431
Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene
Authors: Meira, LB Graham, JM Greenberg, CR Busch, DB Doughty, ATB Ziffer, DW Coleman, DM Savre-Train, I Friedberg, EC
Citation: Lb. Meira et al., Manitoba aboriginal kindred with original cerebro-oculo-facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene, AM J HU GEN, 66(4), 2000, pp. 1221-1228
PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome
Authors: Marsh, DJ Kum, JB Lunetta, KL Bennett, MJ Gorlin, RJ Ahmed, SF Bodurtha, J Crowe, C Curtis, MA Dasouki, M Dunn, T Feit, H Geraghty, MT Graham, JM Hodgson, SV Hunter, A Korf, BR Manchester, D Miesfeldt, S Murday, VA Nathanson, KL Parisi, M Pober, B Romano, C Tolmie, JL Trembath, R Winter, RM Zackai, EH Zori, RT Weng, LP Dahia, PLM Eng, C
Citation: Dj. Marsh et al., PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome, HUM MOL GEN, 8(8), 1999, pp. 1461-1472
The spectrum of mutations in UBE3A causing Angelman syndrome
Authors: Fang, P Lev-Lehman, E Tsai, TF Matsuura, T Benton, CS Sutcliffe, JS Christian, SL Kubota, T Halley, DJ Meijers-Heijboer, H Langlois, S Graham, JM Beuten, J Willems, PJ Ledbetter, DH Beaudet, AL
Citation: P. Fang et al., The spectrum of mutations in UBE3A causing Angelman syndrome, HUM MOL GEN, 8(1), 1999, pp. 129-135
Risultati: 1-25 | 26-34