-
2
-
-
0034956576
-
Electrospray tandem mass spectrometry for acylcarnitines in dried post mortem blood specimens collected at autopsy from infants with unexplained cause of death
-
Chace DH, DiPerna JC, Mitchell BL, Sgroi B, Hofman LF, Naylor EW. Electrospray tandem mass spectrometry for acylcarnitines in dried post mortem blood specimens collected at autopsy from infants with unexplained cause of death. Clin Chem 2001; 47: 1166-82
-
(2001)
Clin Chem
, vol.47
, pp. 1166-1182
-
-
Chace, D.H.1
DiPerna, J.C.2
Mitchell, B.L.3
Sgroi, B.4
Hofman, L.F.5
Naylor, E.W.6
-
3
-
-
0034949696
-
The metabolic autopsy comes of age
-
Bennett MJ, Rinaldo P. The metabolic autopsy comes of age. Clin Chem 2001; 47: 1145-6
-
(2001)
Clin Chem
, vol.47
, pp. 1145-1146
-
-
Bennett, M.J.1
Rinaldo, P.2
-
4
-
-
0242468940
-
Benchtop mass spectrometry in clinical biochemistry
-
Honour JW. Benchtop mass spectrometry in clinical biochemistry. Ann Clin Biochem 2003; 40: 628-38
-
(2003)
Ann Clin Biochem
, vol.40
, pp. 628-638
-
-
Honour, J.W.1
-
5
-
-
0035241692
-
Mass spectrometry in the clinical laboratory
-
Chace DH. Mass spectrometry in the clinical laboratory. Chem Rev 2001; 101: 445-77
-
(2001)
Chem Rev
, vol.101
, pp. 445-477
-
-
Chace, D.H.1
-
6
-
-
0034641566
-
Inborn errors of metabolism around the time of birth
-
Leonard JV, Morris AAM. Inborn errors of metabolism around the time of birth. Lancet 2000; 356: 583-7
-
(2000)
Lancet
, vol.356
, pp. 583-587
-
-
Leonard, J.V.1
Morris, A.A.M.2
-
7
-
-
0002361235
-
Observations on the pathological anatomy of the sudden infant death syndrome
-
Bergman AB, Beckwith JB, Ray CG, eds. Seattle: University of Washington Press
-
Beckwith JB. Observations on the pathological anatomy of the sudden infant death syndrome. In: Bergman AB, Beckwith JB, Ray CG, eds. Sudden Infant Death Syndrome. Seattle: University of Washington Press, 1970: 83-102
-
(1970)
Sudden Infant Death Syndrome
, pp. 83-102
-
-
Beckwith, J.B.1
-
8
-
-
0035421817
-
Sudden infant death syndrome and other causes of infant mortality
-
Hunt CE. Sudden infant death syndrome and other causes of infant mortality. Am J Respir Crit Care Med 2001; 164: 346-57
-
(2001)
Am J Respir Crit Care Med
, vol.164
, pp. 346-357
-
-
Hunt, C.E.1
-
9
-
-
0002695815
-
A clinical comparison of SIDS and unexplained sudden infant deaths: How healthy and how normal?
-
The CESDI SUDI Research Group
-
Platt MW, Blair PS, Fleming PJ, Smith IJ, Cole TJ, Leach CE, et al. The CESDI SUDI Research Group. A clinical comparison of SIDS and unexplained sudden infant deaths: how healthy and how normal? Arch Dis Child 2000; 82: 98-106
-
(2000)
Arch Dis Child
, vol.82
, pp. 98-106
-
-
Platt, M.W.1
Blair, P.S.2
Fleming, P.J.3
Smith, I.J.4
Cole, T.J.5
Leach, C.E.6
-
10
-
-
0033497543
-
Sudden unexplained deaths in infancy: What are the causes?
-
Cote A, Russo P, Michaud J. Sudden unexplained deaths in infancy: what are the causes? J Pediatr 1999; 135: 437-43
-
(1999)
J Pediatr
, vol.135
, pp. 437-443
-
-
Cote, A.1
Russo, P.2
Michaud, J.3
-
11
-
-
0017159824
-
Evidence of duration and type of illness in children found unexpectedly dead
-
Sinclair-Smith C, Dinsdale F, Emery J. Evidence of duration and type of illness in children found unexpectedly dead. Arch Dis Child 1976; 51: 424-8
-
(1976)
Arch Dis Child
, vol.51
, pp. 424-428
-
-
Sinclair-Smith, C.1
Dinsdale, F.2
Emery, J.3
-
12
-
-
0000547499
-
Clinical phenotypes: Diagnosis/algorithms
-
Scriver CR, Beaudet AL, Sly WS, Valle D, eds. New York: McGraw-Hill
-
Saudubray J-M, Charpentier C. Clinical phenotypes: diagnosis/algorithms. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Basis of Inherited Disease, 8th edn. New York: McGraw-Hill, 2000: 1327-403
-
(2000)
The Metabolic and Molecular Basis of Inherited Disease, 8th Edn.
, pp. 1327-1403
-
-
Saudubray, J.-M.1
Charpentier, C.2
-
13
-
-
0036932078
-
Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome
-
Nassogne M-C, Sharrard M, Hertz-Pannier L, Armengaud D, Touati G, Delonlay-Debeney P, et al. Massive subdural haematomas in Menkes disease mimicking shaken baby syndrome. Childs Nerv Syst 2002; 18: 729-31
-
(2002)
Childs Nerv Syst
, vol.18
, pp. 729-731
-
-
Nassogne, M.-C.1
Sharrard, M.2
Hertz-Pannier, L.3
Armengaud, D.4
Touati, G.5
Delonlay-Debeney, P.6
-
14
-
-
0027400082
-
Osteogenesis imperfecta: The distinction from child abuse and the recognition of a variant form
-
Paterson CR, Burns J, McAllion SJ. Osteogenesis imperfecta: the distinction from child abuse and the recognition of a variant form. Am J Med Genet 1993; 45: 187-92
-
(1993)
Am J Med Genet
, vol.45
, pp. 187-192
-
-
Paterson, C.R.1
Burns, J.2
McAllion, S.J.3
-
15
-
-
0036089145
-
Testing for osteogenesis imperfecta in cases of non-accidental injury
-
Marlowe A, Pepin MG, Byers PH. Testing for osteogenesis imperfecta in cases of non-accidental injury. J Med Genet 2002; 39: 382-6
-
(2002)
J Med Genet
, vol.39
, pp. 382-386
-
-
Marlowe, A.1
Pepin, M.G.2
Byers, P.H.3
-
16
-
-
0029013354
-
The rarer coagulation disorders: A review
-
Bolton-Maggs PH, Hill FG. The rarer coagulation disorders: a review. Blood Rev 1995; 9: 65-76
-
(1995)
Blood Rev
, vol.9
, pp. 65-76
-
-
Bolton-Maggs, P.H.1
Hill, F.G.2
-
17
-
-
8944233364
-
Clinical course early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency
-
Hoffman GF, Athanassopoulos S, Burlina AB, Duran M, deKlerk JB, Lehnert W, et al. Clinical course early diagnosis, treatment, and prevention of disease in glutaryl-CoA dehydrogenase deficiency. Neuropediatrics 1996; 27: 115-23
-
(1996)
Neuropediatrics
, vol.27
, pp. 115-123
-
-
Hoffman, G.F.1
Athanassopoulos, S.2
Burlina, A.B.3
Duran, M.4
DeKlerk, J.B.5
Lehnert, W.6
-
18
-
-
0030992936
-
Head injury: Abuse or accident?
-
Wilkins B. Head injury: abuse or accident? Arch Dis Child 1997; 76: 393-7
-
(1997)
Arch Dis Child
, vol.76
, pp. 393-397
-
-
Wilkins, B.1
-
19
-
-
0035186461
-
Glutaric aciduria type I and non-accidental head injury
-
Hartley LM, Khwaja OS, Verity CM. Glutaric aciduria type I and non-accidental head injury. Pediatrics 2001; 107: 174-5
-
(2001)
Pediatrics
, vol.107
, pp. 174-175
-
-
Hartley, L.M.1
Khwaja, O.S.2
Verity, C.M.3
-
20
-
-
0021795143
-
Defects in the metabolism of fatty acids in sudden infant death syndrome
-
Howat AJ, Bennett MJ, Variend S, Shaw L, Engel PC. Defects in the metabolism of fatty acids in sudden infant death syndrome. BMJ 1985; 290: 1771-3
-
(1985)
BMJ
, vol.290
, pp. 1771-1773
-
-
Howat, A.J.1
Bennett, M.J.2
Variend, S.3
Shaw, L.4
Engel, P.C.5
-
21
-
-
0032953017
-
Sudden and unexpected neonatal death: Protocol for the post mortem diagnosis of fatty acid oxidation disorders
-
Rinaldo P, Yoon HR, Yu C, Raymond K, Tiozzo C, Giordano G. Sudden and unexpected neonatal death: protocol for the post mortem diagnosis of fatty acid oxidation disorders. Semin Perinatol 1999; 23: 204-10
-
(1999)
Semin Perinatol
, vol.23
, pp. 204-210
-
-
Rinaldo, P.1
Yoon, H.R.2
Yu, C.3
Raymond, K.4
Tiozzo, C.5
Giordano, G.6
-
22
-
-
0027167804
-
Prevalence of medium-chain dehydrogenase deficiency in sudden infant death syndrome
-
Arens R, Gozel D, Jain K, Muscati S, Heuser ET, Williams JC, et al. Prevalence of medium-chain dehydrogenase deficiency in sudden infant death syndrome. J Pediatr 1993; 122: 715-8
-
(1993)
J Pediatr
, vol.122
, pp. 715-718
-
-
Arens, R.1
Gozel, D.2
Jain, K.3
Muscati, S.4
Heuser, E.T.5
Williams, J.C.6
-
23
-
-
17644435180
-
Retrospective biochemical screening of fatty acid oxidation disorders in post-mortem livers of 418 cases of sudden death in the first year of life
-
Boles RG, Buck EA, Blitzer MG, Platt MS, Cowan TM, Martin SK, et al. Retrospective biochemical screening of fatty acid oxidation disorders in post-mortem livers of 418 cases of sudden death in the first year of life. J Pediatr 1998; 132: 924-33
-
(1998)
J Pediatr
, vol.132
, pp. 924-933
-
-
Boles, R.G.1
Buck, E.A.2
Blitzer, M.G.3
Platt, M.S.4
Cowan, T.M.5
Martin, S.K.6
-
24
-
-
0020363432
-
In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: Evidence of a defect in general acyl-CoA dehydrogenase
-
Kolvraa S, Gregersen N, Christiensen E, Hobolth N. In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence of a defect in general acyl-CoA dehydrogenase. Clin Chim Acta 1982; 126: 53-67
-
(1982)
Clin Chim Acta
, vol.126
, pp. 53-67
-
-
Kolvraa, S.1
Gregersen, N.2
Christiensen, E.3
Hobolth, N.4
-
25
-
-
0020570022
-
14C] octanoate oxidation and medium chain acyl-CoA dehydrogenase deficiency in fibroblasts
-
14C] octanoate oxidation and medium chain acyl-CoA dehydrogenase deficiency in fibroblasts. Science 1983; 221: 73-5
-
(1983)
Science
, vol.221
, pp. 73-75
-
-
Rhead, W.J.1
Amendt, B.A.2
Fritchman, K.S.3
Felts, S.J.4
-
26
-
-
0028265830
-
Medium-chain acyl-CoA dehydrogenase deficiency: Clinical course in 120 affected children
-
Lafolla AK, Thompson RJ Jr, Roe CR. Medium-chain acyl-CoA dehydrogenase deficiency: clinical course in 120 affected children. J Pediatr 1994; 124: 409-15
-
(1994)
J Pediatr
, vol.124
, pp. 409-415
-
-
Lafolla, A.K.1
Thompson Jr., R.J.2
Roe, C.R.3
-
27
-
-
8244255920
-
The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: Is there a correlation between genotype and phenotype?
-
Andresen BS, Bross P, Udvari S, Kirk J, Gray RGF, Kmock S, et al. The molecular basis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in compound heterozygous patients: is there a correlation between genotype and phenotype? Hum Mol Genet 1997; 6: 695-707
-
(1997)
Hum Mol Genet
, vol.6
, pp. 695-707
-
-
Andresen, B.S.1
Bross, P.2
Udvari, S.3
Kirk, J.4
Gray, R.G.F.5
Kmock, S.6
-
28
-
-
0033224545
-
Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review
-
Wang SS, Fernhoff PM, Hannon WH, Khoury MJ. Medium chain acyl-CoA dehydrogenase deficiency human genome epidemiology review. Genet Med 1999; 1: 332-9
-
(1999)
Genet Med
, vol.1
, pp. 332-339
-
-
Wang, S.S.1
Fernhoff, P.M.2
Hannon, W.H.3
Khoury, M.J.4
-
29
-
-
0028208537
-
Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency
-
Heales SJR, Thompson GN, Massoud AF, Rahman S, Halliday D, Leonard JV. Production and disposal of medium-chain fatty acids in children with medium-chain acyl-CoA dehydrogenase deficiency. J Inherit Metab Dis 1994; 17: 74-80
-
(1994)
J Inherit Metab Dis
, vol.17
, pp. 74-80
-
-
Heales, S.J.R.1
Thompson, G.N.2
Massoud, A.F.3
Rahman, S.4
Halliday, D.5
Leonard, J.V.6
-
30
-
-
0035112892
-
Fasting medium chain acyl-CoA dehydrogenase-deficient children can make ketones
-
Fletcher JM, Pitt JJ. Fasting medium chain acyl-CoA dehydrogenase- deficient children can make ketones. Metabolism 2001; 50: 161-5
-
(2001)
Metabolism
, vol.50
, pp. 161-165
-
-
Fletcher, J.M.1
Pitt, J.J.2
-
33
-
-
0028067548
-
A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death
-
Brackett JC, Sims HF, Steiner RD, Nunge M, Zimmerman EM, deMartinville B, et al. A novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death. J Clin Invest 1994; 94: 1477-83
-
(1994)
J Clin Invest
, vol.94
, pp. 1477-1483
-
-
Brackett, J.C.1
Sims, H.F.2
Steiner, R.D.3
Nunge, M.4
Zimmerman, E.M.5
DeMartinville, B.6
-
34
-
-
0028949363
-
Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency
-
Ruitenbeek W, Poelis PJ, Turnbull DM, Garavaglia B, Chalmers RA, Taylor RW, et al. Rhabdomyolysis and acute encephalopathy in late onset medium chain acyl-CoA dehydrogenase deficiency. J Neurol Neurosurg Psychiatry 1995; 58: 209-14
-
(1995)
J Neurol Neurosurg Psychiatry
, vol.58
, pp. 209-214
-
-
Ruitenbeek, W.1
Poelis, P.J.2
Turnbull, D.M.3
Garavaglia, B.4
Chalmers, R.A.5
Taylor, R.W.6
-
35
-
-
1042293127
-
Medium chain acyl-CoA dehydrogenase deficiency: Sudden and unexpected death of a 45 year old woman
-
Rinaldo P, Raymond K, Barnes CA. Medium chain acyl-CoA dehydrogenase deficiency: sudden and unexpected death of a 45 year old woman. J Inherit Metab Dis 1999; 22: 104
-
(1999)
J Inherit Metab Dis
, vol.22
, pp. 104
-
-
Rinaldo, P.1
Raymond, K.2
Barnes, C.A.3
-
36
-
-
0026010499
-
Specific diagnosis of medium chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point mutation (G985) in the MCAD gene
-
Gregerson N, Blakemore A, Winter V, Andresen BS, Kolvraa S, Bolund L, et al. Specific diagnosis of medium chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point mutation (G985) in the MCAD gene. Clin Chim Acta 1991; 203: 23-34
-
(1991)
Clin Chim Acta
, vol.203
, pp. 23-34
-
-
Gregerson, N.1
Blakemore, A.2
Winter, V.3
Andresen, B.S.4
Kolvraa, S.5
Bolund, L.6
-
38
-
-
0033004986
-
Recognition and management of fatty acid oxidation defects: A series of 107 patients
-
Saudubray JM, Martin D, de Lonlay P, Touati G, Poggi-Travert F, Bonnet D, et al. Recognition and management of fatty acid oxidation defects: a series of 107 patients. J Inherit Metab Dis 1999; 22: 448-502
-
(1999)
J Inherit Metab Dis
, vol.22
, pp. 448-502
-
-
Saudubray, J.M.1
Martin, D.2
De Lonlay, P.3
Touati, G.4
Poggi-Travert, F.5
Bonnet, D.6
-
39
-
-
1042293128
-
Late-presenting carnitine transport defect
-
Pollitt RJ, Olpin SE, Bonham JR, Cahalane SF, Naughten E. Late-presenting carnitine transport defect. Enzyme Protein 1993; 47: 175
-
(1993)
Enzyme Protein
, vol.47
, pp. 175
-
-
Pollitt, R.J.1
Olpin, S.E.2
Bonham, J.R.3
Cahalane, S.F.4
Naughten, E.5
-
40
-
-
0033506343
-
Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis
-
Maestri NE, Clissold DB, Brusilow S. Neonatal onset ornithine transcarbamylase deficiency: a retrospective analysis. J Pediatr 1999; 134: 268-72
-
(1999)
J Pediatr
, vol.134
, pp. 268-272
-
-
Maestri, N.E.1
Clissold, D.B.2
Brusilow, S.3
-
41
-
-
0022178203
-
Differentiation of transient hyperammonaemia of the newborn and urea cycle enzyme defects by clinical presentation
-
Hudak ML, Jones MD, Brusilow SW. Differentiation of transient hyperammonaemia of the newborn and urea cycle enzyme defects by clinical presentation. J Pediatr 1985; 107: 712-9
-
(1985)
J Pediatr
, vol.107
, pp. 712-719
-
-
Hudak, M.L.1
Jones, M.D.2
Brusilow, S.W.3
-
42
-
-
0002224776
-
Clinical presentation of respiratory chain deficiency
-
Scriver CR, Beaudet AL, Sly WS, Valle D, eds. New York: McGraw-Hill
-
Munnich A, Rotig A, Cormier-Daire V, Rustin P. Clinical presentation of respiratory chain deficiency. In: Scriver CR, Beaudet AL, Sly WS, Valle D, eds. The Metabolic and Molecular Basis of Inherited Disease, 8th edn. New York: McGraw-Hill, 2000: 2261-74
-
(2000)
The Metabolic and Molecular Basis of Inherited Disease, 8th Edn.
, pp. 2261-2274
-
-
Munnich, A.1
Rotig, A.2
Cormier-Daire, V.3
Rustin, P.4
-
43
-
-
0037639877
-
Expanded newborn screening for inborn errors of metabolism by electrospray ionisation-tandem mass spectrometry: Results, outcome, and implications
-
Schulze A, Lindner M, Kohlmuller D, Olgemoller K, Mayatepek E, Hoffmann GF. Expanded newborn screening for inborn errors of metabolism by electrospray ionisation-tandem mass spectrometry: results, outcome, and implications. Pediatrics 2003; 111: 1399-406
-
(2003)
Pediatrics
, vol.111
, pp. 1399-1406
-
-
Schulze, A.1
Lindner, M.2
Kohlmuller, D.3
Olgemoller, K.4
Mayatepek, E.5
Hoffmann, G.F.6
-
44
-
-
0030883787
-
The genetics of dilated cardiomyopathy: Emerging clues to the puzzle
-
Leiden JM. The genetics of dilated cardiomyopathy: emerging clues to the puzzle. N Engl J Med 1997; 337: 1080-1
-
(1997)
N Engl J Med
, vol.337
, pp. 1080-1081
-
-
Leiden, J.M.1
-
45
-
-
0027931039
-
Biochemical and molecular investigations in respiratory chain deficiencies
-
Rustin P, Chretien D, Bourgeron T, Gerard B, Rotig A, Saudubray JM, et al. Biochemical and molecular investigations in respiratory chain deficiencies. Clin Chim Acta 1994; 228: 35-51
-
(1994)
Clin Chim Acta
, vol.228
, pp. 35-51
-
-
Rustin, P.1
Chretien, D.2
Bourgeron, T.3
Gerard, B.4
Rotig, A.5
Saudubray, J.M.6
-
46
-
-
0022487208
-
Respiratory chain defects in the mitochondria of cultured fibroblasts from three patients with lacticacidaemia
-
Robinson BH, Ward J, Goodyer P, Baudet A. Respiratory chain defects in the mitochondria of cultured fibroblasts from three patients with lacticacidaemia. J Clin Invest 1986; 77: 1422-7
-
(1986)
J Clin Invest
, vol.77
, pp. 1422-1427
-
-
Robinson, B.H.1
Ward, J.2
Goodyer, P.3
Baudet, A.4
-
47
-
-
0025123850
-
The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lactic acidaemia
-
Robinson BH, Glerum DM, Chow W, Petrova-Benedict R, Lightowlers R, Capaldi R. The use of skin fibroblast cultures in the detection of respiratory chain defects in patients with lactic acidaemia. Pediatr Res 1990; 28: 549-55
-
(1990)
Pediatr Res
, vol.28
, pp. 549-555
-
-
Robinson, B.H.1
Glerum, D.M.2
Chow, W.3
Petrova-Benedict, R.4
Lightowlers, R.5
Capaldi, R.6
-
48
-
-
0023100360
-
Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase. Clues to pathogenesis of Leigh disease
-
Robinson BH, De Meirlier L, Glerum P, Sherwood G, Becker L. Clinical presentation of mitochondrial respiratory chain defects in NADH-coenzyme Q reductase and cytochrome oxidase. Clues to pathogenesis of Leigh disease. J Pediatr 1987; 110: 216-22
-
(1987)
J Pediatr
, vol.110
, pp. 216-222
-
-
Robinson, B.H.1
De Meirlier, L.2
Glerum, P.3
Sherwood, G.4
Becker, L.5
-
49
-
-
0034857393
-
Leigh disease: Clinical, neuroradiological, and biochemical study of three new cases with cytochrome c oxidase deficiency
-
Savasta S, Comi GP, Perini MP, Lupi A, Strazzer S, Rognoni F, et al. Leigh disease: clinical, neuroradiological, and biochemical study of three new cases with cytochrome c oxidase deficiency. J Clin Neurol 2001; 16: 608-13
-
(2001)
J Clin Neurol
, vol.16
, pp. 608-613
-
-
Savasta, S.1
Comi, G.P.2
Perini, M.P.3
Lupi, A.4
Strazzer, S.5
Rognoni, F.6
-
50
-
-
0032732526
-
Recent developments in the investigation of inherited metabolic disorders using cultured human cells
-
Roe CR, Roe DS. Recent developments in the investigation of inherited metabolic disorders using cultured human cells. Mol Genet Metab 1999; 68: 243-57
-
(1999)
Mol Genet Metab
, vol.68
, pp. 243-257
-
-
Roe, C.R.1
Roe, D.S.2
-
51
-
-
0030808290
-
3H]Oleic acid: For the improved detection of long chain fatty acid oxidation defects in intact cells
-
3H]Oleic acid: for the improved detection of long chain fatty acid oxidation defects in intact cells. J Inherit Metab Dis 1997; 20: 415-9
-
(1997)
J Inherit Metab Dis
, vol.20
, pp. 415-419
-
-
Olpin, S.E.1
Manning, N.J.2
Pollitt, R.J.3
Clarke, S.4
-
52
-
-
0028950214
-
Evidence for intermediate channeling in mitochondrial beta-oxidation
-
Nada MA, Rhead WJ, Sprecher H, Schulz H, Roe CR. Evidence for intermediate channeling in mitochondrial beta-oxidation. J Biol Chem 1995; 270: 530-5
-
(1995)
J Biol Chem
, vol.270
, pp. 530-535
-
-
Nada, M.A.1
Rhead, W.J.2
Sprecher, H.3
Schulz, H.4
Roe, C.R.5
|