PubMed

Brain phosphoinositide extraction, fractionation, and analysis by MALDI-TOF MS.

Johanson RA, Berry GT.

Methods Mol Biol. 2009;579:189-200.PMID: 19763476 [PubMed - in process]Related articles

Knockout mice in understanding the mechanism of action of lithium.

Agam G, Bersudsky Y, Berry GT, Moechars D, Lavi-Avnon Y, Belmaker RH.

Biochem Soc Trans. 2009 Oct;37(Pt 5):1121-5.PMID: 19754464 [PubMed - in process]Related articles

The unexplored potential of the pentose phosphate pathway in health and disease.

Berry GT.

J Inherit Metab Dis. 2008 Dec;31(6):661. No abstract available. PMID: 19015949 [PubMed - indexed for MEDLINE]Related articles

Characterization of the null murine sodium/myo-inositol cotransporter 1 (Smit1 or Slc5a3) phenotype: myo-inositol rescue is independent of expression of its cognate mitochondrial ribosomal protein subunit 6 (Mrps6) gene and of phosphatidylinositol levels in neonatal brain.

Buccafusca R, Venditti CP, Kenyon LC, Johanson RA, Van Bockstaele E, Ren J, Pagliardini S, Minarcik J, Golden JA, Coady MJ, Greer JJ, Berry GT.

Mol Genet Metab. 2008 Sep-Oct;95(1-2):81-95.PMID: 18675571 [PubMed - indexed for MEDLINE]Related articles

Metabolic profiling.

Berry GT.

Nestle Nutr Workshop Ser Pediatr Program. 2008;62:55-75; discussion 75-80. Review.PMID: 18626193 [PubMed - indexed for MEDLINE]Related articles

Galactosemia and amenorrhea in the adolescent.

Berry GT.

Ann N Y Acad Sci. 2008;1135:112-7. Review.PMID: 18574215 [PubMed - indexed for MEDLINE]Related articles

Homozygote inositol transporter knockout mice show a lithium-like phenotype.

Bersudsky Y, Shaldubina A, Agam G, Berry GT, Belmaker RH.

Bipolar Disord. 2008 Jun;10(4):453-9.PMID: 18452441 [PubMed - indexed for MEDLINE]Related articles

Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin.

Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Vockley J, Berry GT, Lamhonwah AM, Matern D, Roe CR, Gregersen N.

Mol Genet Metab. 2008 Feb;93(2):179-89. Epub 2007 Dec 3.PMID: 18054510 [PubMed - indexed for MEDLINE]Related articles

Survival after treatment with phenylacetate and benzoate for urea-cycle disorders.

Enns GM, Berry SA, Berry GT, Rhead WJ, Brusilow SW, Hamosh A.

N Engl J Med. 2007 May 31;356(22):2282-92.PMID: 17538087 [PubMed - indexed for MEDLINE]Related articlesFree article

Phosphatidylcholine removal from brain lipid extracts expands lipid detection and enhances phosphoinositide quantification by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry.

Johanson RA, Buccafusca R, Quong JN, Shaw MA, Berry GT.

Anal Biochem. 2007 Mar 15;362(2):155-67. Epub 2006 Dec 20.PMID: 17266916 [PubMed - indexed for MEDLINE]Related articles

REMOVED: Short-chain acyl-CoA dehydrogenase gene mutation (319 C>T) presents with clinical heterogeneity and is candidate founder mutation in Ashkenazi Jewish population.

Tein I, Elpeleg O, Ben-Zeev B, Korman SH, Lossos A, Lev D, Lerman-Sagie T, Vockley G, Berry GT, Lamhownah AM, Matern D, Roe CR, Gregersen N.

Mol Genet Metab. 2007 Jan 17. [Epub ahead of print]PMID: 17234443 [PubMed - as supplied by publisher]Related articles

Behavioural phenotyping of sodium-myo-inositol cotransporter heterozygous knockout mice with reduced brain inositol.

Shaldubina A, Buccafusca R, Johanson RA, Agam G, Belmaker RH, Berry GT, Bersudsky Y.

Genes Brain Behav. 2007 Apr;6(3):253-9. Epub 2006 Jul 17.PMID: 16848785 [PubMed - indexed for MEDLINE]Related articles

Liver transplantation is not curative for methylmalonic acidopathy caused by methylmalonyl-CoA mutase deficiency.

Kaplan P, Ficicioglu C, Mazur AT, Palmieri MJ, Berry GT.

Mol Genet Metab. 2006 Aug;88(4):322-6. Epub 2006 Jun 5.PMID: 16750411 [PubMed - indexed for MEDLINE]Related articles

SMIT1 haploinsufficiency causes brain inositol deficiency without affecting lithium-sensitive behavior.

Shaldubina A, Johanson RA, O'Brien WT, Buccafusca R, Agam G, Belmaker RH, Klein PS, Bersudsky Y, Berry GT.

Mol Genet Metab. 2006 Aug;88(4):384-8. Epub 2006 Apr 27.PMID: 16644257 [PubMed - indexed for MEDLINE]Related articles

Epimerase-deficiency galactosemia is not a binary condition.

Openo KK, Schulz JM, Vargas CA, Orton CS, Epstein MP, Schnur RE, Scaglia F, Berry GT, Gottesman GS, Ficicioglu C, Slonim AE, Schroer RJ, Yu C, Rangel VE, Keenan J, Lamance K, Fridovich-Keil JL.

Am J Hum Genet. 2006 Jan;78(1):89-102. Epub 2005 Nov 14.PMID: 16385452 [PubMed - indexed for MEDLINE]Related articlesFree article

Elements of diabetic nephropathy in a patient with GLUT 2 deficiency.

Berry GT, Baynes JW, Wells-Knecht KJ, Szwergold BS, Santer R.

Mol Genet Metab. 2005 Dec;86(4):473-7. Epub 2005 Nov 8.PMID: 16288895 [PubMed - indexed for MEDLINE]Related articles

Congenital cardiomyopathy and pulmonary hypertension: another fatal variant of cytochrome-c oxidase deficiency.

Venditti CP, Harris MC, Huff D, Peterside I, Munson D, Weber HS, Rome J, Kaye EM, Shanske S, Sacconi S, Tay S, DiMauro S, Berry GT.

J Inherit Metab Dis. 2004;27(6):735-9.PMID: 15505378 [PubMed - indexed for MEDLINE]Related articles

Extended [13C]galactose oxidation studies in patients with galactosemia.

Berry GT, Reynolds RA, Yager CT, Segal S.

Mol Genet Metab. 2004 Jun;82(2):130-6.PMID: 15172000 [PubMed - indexed for MEDLINE]Related articles

Phosphoinositide deficiency due to inositol depletion is not a mechanism of lithium action in brain.

Berry GT, Buccafusca R, Greer JJ, Eccleston E.

Mol Genet Metab. 2004 May;82(1):87-92. Erratum in: Mol Genet Metab. 2004 Dec;83(4):348. PMID: 15110328 [PubMed - indexed for MEDLINE]Related articles

The rate of de novo galactose synthesis in patients with galactose-1-phosphate uridyltransferase deficiency.

Berry GT, Moate PJ, Reynolds RA, Yager CT, Ning C, Boston RC, Segal S.

Mol Genet Metab. 2004 Jan;81(1):22-30.PMID: 14728988 [PubMed - indexed for MEDLINE]Related articles

Newborn screening by tandem mass spectrometry for medium-chain Acyl-CoA dehydrogenase deficiency: a cost-effectiveness analysis.

Venditti LN, Venditti CP, Berry GT, Kaplan PB, Kaye EM, Glick H, Stanley CA.

Pediatrics. 2003 Nov;112(5):1005-15.PMID: 14595039 [PubMed - indexed for MEDLINE]Related articlesFree article

In vivo pyruvate detected by MR spectroscopy in neonatal pyruvate dehydrogenase deficiency.

Zand DJ, Simon EM, Pulitzer SB, Wang DJ, Wang ZJ, Rorke LB, Palmieri M, Berry GT.

AJNR Am J Neuroradiol. 2003 Aug;24(7):1471-4.PMID: 12917150 [PubMed - indexed for MEDLINE]Related articlesFree article

Clinical spectrum of succinic semialdehyde dehydrogenase deficiency.

Pearl PL, Gibson KM, Acosta MT, Vezina LG, Theodore WH, Rogawski MA, Novotny EJ, Gropman A, Conry JA, Berry GT, Tuchman M.

Neurology. 2003 May 13;60(9):1413-7.PMID: 12743223 [PubMed - indexed for MEDLINE]Related articles

Ataxia-telangiectasia: the pattern of cerebellar atrophy on MRI.

Tavani F, Zimmerman RA, Berry GT, Sullivan K, Gatti R, Bingham P.

Neuroradiology. 2003 May;45(5):315-9. Epub 2003 Apr 11.PMID: 12740724 [PubMed - indexed for MEDLINE]Related articles

MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensation.

Jan W, Zimmerman RA, Wang ZJ, Berry GT, Kaplan PB, Kaye EM.

Neuroradiology. 2003 Jun;45(6):393-9. Epub 2003 May 8.PMID: 12736767 [PubMed - indexed for MEDLINE]Related articles

Loss of murine Na+/myo-inositol cotransporter leads to brain myo-inositol depletion and central apnea.

Berry GT, Wu S, Buccafusca R, Ren J, Gonzales LW, Ballard PL, Golden JA, Stevens MJ, Greer JJ.

J Biol Chem. 2003 May 16;278(20):18297-302. Epub 2003 Feb 11.PMID: 12582158 [PubMed - indexed for MEDLINE]Related articlesFree article

Biliary atresia associated with a fatty acid oxidation defect.

Matthews RP, Russo P, Berry GT, Piccoli DA, Rand EB.

J Pediatr Gastroenterol Nutr. 2002 Nov;35(5):624-8. No abstract available. PMID: 12454576 [PubMed - indexed for MEDLINE]Related articles

The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome.

Santer R, Groth S, Kinner M, Dombrowski A, Berry GT, Brodehl J, Leonard JV, Moses S, Norgren S, Skovby F, Schneppenheim R, Steinmann B, Schaub J.

Hum Genet. 2002 Jan;110(1):21-9. Epub 2001 Nov 17.PMID: 11810292 [PubMed - indexed for MEDLINE]Related articles

Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiency.

Berry GT, Fukao T, Mitchell GA, Mazur A, Ciafre M, Gibson J, Kondo N, Palmieri MJ.

J Inherit Metab Dis. 2001 Oct;24(5):587-95.PMID: 11757586 [PubMed - indexed for MEDLINE]Related articles

Proton magnetic resonance spectroscopy of brain metabolites in galactosemia.

Wang ZJ, Berry GT, Dreha SF, Zhao H, Segal S, Zimmerman RA.

Ann Neurol. 2001 Aug;50(2):266-9.PMID: 11506413 [PubMed - indexed for MEDLINE]Related articles

Reversible subacute combined degeneration of the spinal cord in a 14-year-old due to a strict vegan diet.

Licht DJ, Berry GT, Brooks DG, Younkin DP.

Clin Pediatr (Phila). 2001 Jul;40(7):413-5. No abstract available. PMID: 11491139 [PubMed - indexed for MEDLINE]Related articles

Evidence for alternate galactose oxidation in a patient with deletion of the galactose-1-phosphate uridyltransferase gene.

Berry GT, Leslie N, Reynolds R, Yager CT, Segal S.

Mol Genet Metab. 2001 Apr;72(4):316-21.PMID: 11286505 [PubMed - indexed for MEDLINE]Related articles

Galactose metabolism in mice with galactose-1-phosphate uridyltransferase deficiency: sucklings and 7-week-old animals fed a high-galactose diet.

Ning C, Reynolds R, Chen J, Yager C, Berry GT, Leslie N, Segal S.

Mol Genet Metab. 2001 Apr;72(4):306-15.PMID: 11286504 [PubMed - indexed for MEDLINE]Related articles

In vivo evidence of brain galactitol accumulation in an infant with galactosemia and encephalopathy.

Berry GT, Hunter JV, Wang Z, Dreha S, Mazur A, Brooks DG, Ning C, Zimmerman RA, Segal S.

J Pediatr. 2001 Feb;138(2):260-2.PMID: 11174626 [PubMed - indexed for MEDLINE]Related articles

Long-term management of patients with urea cycle disorders.

Berry GT, Steiner RD.

J Pediatr. 2001 Jan;138(1 Suppl):S56-60; discussion S60-1.PMID: 11148550 [PubMed - indexed for MEDLINE]Related articles

Ornithine transcarbamylase deficiency and pancreatitis.

Anadiotis G, Ierardi-Curto L, Kaplan PB, Berry GT.

J Pediatr. 2001 Jan;138(1):123-4.PMID: 11148526 [PubMed - indexed for MEDLINE]Related articles

Risk factors for premature ovarian failure in females with galactosemia.

Guerrero NV, Singh RH, Manatunga A, Berry GT, Steiner RD, Elsas LJ 2nd.

J Pediatr. 2000 Dec;137(6):833-41.PMID: 11113841 [PubMed - indexed for MEDLINE]Related articles

Apparent galactose appearance rate in human galactosemia based on plasma [(13)C]galactose isotopic enrichment.

Ning C, Fenn PT, Blair IA, Berry GT, Segal S.

Mol Genet Metab. 2000 Aug;70(4):261-71.PMID: 10993713 [PubMed - indexed for MEDLINE]Related articles

Succinyl-CoA:3-ketoacid CoA transferase (SCOT): cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations.

Fukao T, Mitchell GA, Song XQ, Nakamura H, Kassovska-Bratinova S, Orii KE, Wraith JE, Besley G, Wanders RJ, Niezen-Koning KE, Berry GT, Palmieri M, Kondo N.

Genomics. 2000 Sep 1;68(2):144-51.PMID: 10964512 [PubMed - indexed for MEDLINE]Related articles

Galactose breath testing distinguishes variant and severe galactose-1-phosphate uridyltransferase genotypes.

Berry GT, Singh RH, Mazur AT, Guerrero N, Kennedy MJ, Chen J, Reynolds R, Palmieri MJ, Klein PD, Segal S, Elsas LJ 2nd.

Pediatr Res. 2000 Sep;48(3):323-8.PMID: 10960497 [PubMed - indexed for MEDLINE]Related articles

Galactose metabolism by the mouse with galactose-1-phosphate uridyltransferase deficiency.

Ning C, Reynolds R, Chen J, Yager C, Berry GT, McNamara PD, Leslie N, Segal S.

Pediatr Res. 2000 Aug;48(2):211-7.PMID: 10926297 [PubMed - indexed for MEDLINE]Related articles

Hyperammonia Possibly due to Corticosteroids.

Berry GT, Kaplan PB, Lichtenstein GR.

Arch Neurol. 2000 Jul;57(7):1085-10856. No abstract available. PMID: 10891999 [PubMed - as supplied by publisher]Related articles

Murine chromosome 16 telomeric region, homologous with human chromosome 21q22, contains the osmoregulatory Na(+)/myo-inositol cotransporter (SLC5A3) gene.

McVeigh KE, Mallee JJ, Lucente A, Barnoski BL, Wu S, Berry GT.

Cytogenet Cell Genet. 2000;88(1-2):153-8.PMID: 10773690 [PubMed - indexed for MEDLINE]Related articles

The glutamine paradox in a neonate with propionic acidaemia and severe hyperammonaemia.

Ierardi-Curto L, Kaplan P, Saitta S, Mazur A, Berry GT.

J Inherit Metab Dis. 2000 Feb;23(1):85-6. No abstract available. PMID: 10682312 [PubMed - indexed for MEDLINE]Related articles

Fatal hyperammonemia after orthotopic lung transplantation.

Lichtenstein GR, Yang YX, Nunes FA, Lewis JD, Tuchman M, Tino G, Kaiser LR, Palevsky HI, Kotloff RM, Furth EE, Bavaria JE, Stecker MM, Kaplan P, Berry GT.

Ann Intern Med. 2000 Feb 15;132(4):283-7.PMID: 10681283 [PubMed - indexed for MEDLINE]Related articlesFree article

Urine and plasma galactitol in patients with galactose-1-phosphate uridyltransferase deficiency galactosemia.

Palmieri M, Mazur A, Berry GT, Ning C, Wehrli S, Yager C, Reynolds R, Singh R, Muralidharan K, Langley S, Elsas L 2nd, Segal S.

Metabolism. 1999 Oct;48(10):1294-302.PMID: 10535394 [PubMed - indexed for MEDLINE]Related articles

A new mitochondrial DNA mutation (A3288G) in the tRNA(Leu(UUR)) gene associated with familial myopathy.

Hadjigeorgiou GM, Kim SH, Fischbeck KH, Andreu AL, Berry GT, Bingham P, Shanske S, Bonilla E, DiMauro S.

J Neurol Sci. 1999 Apr 1;164(2):153-7.PMID: 10402027 [PubMed - indexed for MEDLINE]Related articles

In vivo brain myo-inositol levels in children with Down syndrome.

Berry GT, Wang ZJ, Dreha SF, Finucane BM, Zimmerman RA.

J Pediatr. 1999 Jul;135(1):94-7.PMID: 10393611 [PubMed - indexed for MEDLINE]Related articles

Successful use of alternate waste nitrogen agents and hemodialysis in a patient with hyperammonemic coma after heart-lung transplantation.

Berry GT, Bridges ND, Nathanson KL, Kaplan P, Clancy RR, Lichtenstein GR, Spray TL.

Arch Neurol. 1999 Apr;56(4):481-4.PMID: 10199339 [PubMed - indexed for MEDLINE]Related articlesFree article

Abnormal myo-inositol and phospholipid metabolism in cultured fibroblasts from patients with ataxia telangiectasia.

Yorek MA, Dunlap JA, Manzo-Fontes A, Bianchi R, Berry GT, Eichberg J.

Biochim Biophys Acta. 1999 Mar 25;1437(3):287-300.PMID: 10101263 [PubMed - indexed for MEDLINE]Related articles