Berry, G.T.
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1

UX007 for the treatment of long chain-fatty acid oxidation ..:

Vockley, J. ; Burton, B. ; Berry, G.T....
Molecular Genetics and Metabolism.  120 (2017)  4 - p. 370-377 , 2017
 
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2

The galactosemia network (GalNet):

Rubio‐Gozalbo, M. E. ; Bosch, A. M. ; Burlina, A....
Journal of Inherited Metabolic Disease.  40 (2016)  2 - p. 169-170 , 2016
 
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3

IP3 accumulation and/or inositol depletion: two downstream ..:

Sade, Y ; Toker, L ; Kara, N Z...
Translational Psychiatry.  6 (2016)  12 - p. e968-e968 , 2016
 
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5

A Type of Hyperelliptic Continued Fraction:

Berry, T. G.
Monatshefte für Mathematik.  145 (2005)  4 - p. 269-283 , 2005
 
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6

Congenital cardiomyopathy and pulmonary hypertension: Anoth..:

Venditti, C. P. ; Harris, M. C. ; Huff, D....
Journal of Inherited Metabolic Disease.  27 (2004)  6 - p. 735-739 , 2004
 
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7

Biquadratic Reciprocity and a Lucasian Primality Test:

Berrizbeitia, Pedro ; Berry, T. G.
Mathematics of Computation.  73 (2004)  247 - p. 1559-1564 , 2004
 
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9

Implicitization and parametrization of nonsingular cubic su..:

Berry, T.G. ; Patterson, Richard R.
Computer Aided Geometric Design.  18 (2001)  8 - p. 723-738 , 2001
 
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10

Neonatal hypoglycaemia in severe succinyl‐CoA:3‐oxoacid CoA..:

Berry, G. T. ; Fukao, T. ; Mitchell, G. A....
Journal of Inherited Metabolic Disease.  24 (2001)  5 - p. 587-595 , 2001
 
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11

Groebner bases of the ideal of a space curve:

Berry, T.G.
Journal of Pure and Applied Algebra.  148 (2000)  1 - p. 17-27 , 2000
 
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12

The glutamine paradox in a neonate with propionic acidaemia..:

Ierardi‐Curto, L. ; Kaplan, P. ; Saitta, S...
Journal of Inherited Metabolic Disease.  23 (2000)  1 - p. 85-86 , 2000
 
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13

Generalized Strong Pseudoprime Tests and Applications:

Berrizbeitia, Pedro ; Berry, T.G.
Journal of Symbolic Computation.  30 (2000)  2 - p. 151-160 , 2000
 
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14

Cubic Reciprocity and Generalised Lucas-Lehmer Tests for Pr..:

Berrizbeitia, Pedro ; Berry, T. G.
Proceedings of the American Mathematical Society.  127 (1999)  7 - p. 1923-1925 , 1999
 
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15

A new mitochondrial DNA mutation (A3288G) in the tRNALeu(UU..:

Hadjigeorgiou, G.M. ; Kim, S.H. ; Fischbeck, K.H....
Journal of the Neurological Sciences.  164 (1999)  2 - p. 153-157 , 1999
 
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