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W. Ruitenbeek

Veröffentlichungen von W. Ruitenbeek zu Ruitenbeek, W.. ->
weitere Veröffentlichungen von W. Ruitenbeek:
The fatty acid composition of various lipid fractions isolated from erythrocytes and blood plasma of patients with duchenne and congenital myotonic muscular dystrophy (1978)
Ethylmalonic aciduria associated with progressive neurological disease and partial cytochromec oxidase deficiency (1993)
Alteration of skeletal muscle during malignant hyperthermia. Fine structural studies and localization of calcium (1984)
Decreased activity of respiratory-chain enzymes in glutaric aciduria type II (1995)
High field de Haas-van alphen effect in the quasi two dimensional metal Hg"3"-"δAsF"6 (1989)
Osmotic stability of erythrocytes in human muscular dystrophy before and after phospholipase treatment (1979)
Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies (1990)
The effect of the oxygen content in Pb"2SrLaCu"2O"6"+"δ and Pb"2Ba"2YCu"3O"8"+"δ on the structural and superconducting properties (1990)
Systemic Infantile Complex I Deficiency with Fatal Outcome in Two Brothers (1998)
Mitochondrial Angiopathy in a Family with MELAS (1992)
Sudden Loss of Hearing and Vestibular Function, Muscular Weakness, and Multiple White Matter Lesions in Preschool Children (1992)
Systemic Infantile Complex I Deficiency with Fatal Outcome in Two Brothers (1998)
Muscle cytochromec oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl-CoA dehydrogenase deficiency (1993)
Enzymological versus DNA investigations in mitochondrial (encephalo-)myopathies (1993)
Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria (1994)
Veröffentlichungen zu Ruitenbeek, W..
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1
Ruitenbeek, W. The fatty acid composition of various lipid fractions isolated from erythrocytes and blood plasma of patients with duchenne and congenital myotonic muscular dystrophy
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 89, No. 1 (1978), p. 99-110
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1978
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2
Lehnert, W., Ruitenbeek, W. Ethylmalonic aciduria associated with progressive neurological disease and partial cytochromec oxidase deficiency
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 16 (3. 1993), p. 557-559
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1993
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3
Viering, W., Stadhouders, A., ... Alteration of skeletal muscle during malignant hyperthermia. Fine structural studies and localization of calcium
in: Ultramicroscopy, in: Ultramicroscopy . - Amsterdam : Elsevier, ISSN 0304-3991, ZDB-ID 1479043-9 Vol. 14, No. 4 (1984), p. 418
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1984
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4
Santer, R., Claaβ, A., ... Decreased activity of respiratory-chain enzymes in glutaric aciduria type II
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 18 (1. 1995), p. 75-76
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1995
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5
van Ruitenbeek, J.M., Joss, W., ... High field de Haas-van alphen effect in the quasi two dimensional metal Hg"3"-"δAsF"6
in: Solid State Communications, in: Solid State Communications . - Amsterdam : Elsevier, ISSN 0038-1098, ZDB-ID 1467698-9 Vol. 71, No. 10 (1989), p. 875-878
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1989
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6
Ruitenbeek, W., Edixhoven, M.J., ... Osmotic stability of erythrocytes in human muscular dystrophy before and after phospholipase treatment
in: Clinica Chimica Acta, in: Clinica Chimica Acta . - Amsterdam : Elsevier, ISSN 0009-8981, ZDB-ID 1499920-1 Vol. 94, No. 3 (1979), p. 259-266
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1979
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7
Sperl, W., Ruitenbeek, W., ... Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 13 (3. 1990), p. 359-362
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1990
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8
Zandbergen, H.W., Fu, W.T., ... The effect of the oxygen content in Pb"2SrLaCu"2O"6"+"δ and Pb"2Ba"2YCu"3O"8"+"δ on the structural and superconducting properties
in: Physica C: Superconductivity and its applications, in: Physica C: Superconductivity and its applications . - Amsterdam : Elsevier, ISSN 0921-4534, ZDB-ID 1467152-9 Vol. 166, No. 5-6 (1990), p. 502-512
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1990
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9
Rubio-Cozalbo, M. E.. Systemic Infantile Complex I Deficiency with Fatal Outcome in Two Brothers
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 29, No. 01 (2. 1998), p. 43-45
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1998
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10
Förster, Ch.. Mitochondrial Angiopathy in a Family with MELAS
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 23, No. 03 (6. 1992), p. 165-168
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1992
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11
Lenard, H. G.. Sudden Loss of Hearing and Vestibular Function, Muscular Weakness, and Multiple White Matter Lesions in Preschool Children
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 23, No. 04 (8. 1992), p. 221-224
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1992
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12
Rubio-Cozalbo, M. E.. Systemic Infantile Complex I Deficiency with Fatal Outcome in Two Brothers
In: Neuropediatrics. - Stuttgart [u.a.] : Thieme Vol. 29, No. 01 (2. 1998), p. 43-45
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1998
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13
Christensen, E., Brandt, N. J., ... Muscle cytochromec oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl-CoA dehydrogenase deficiency
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 16 (3. 1993), p. 553-556
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1993
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14
Vries, D. D., Ruitenbeek, W., ... Enzymological versus DNA investigations in mitochondrial (encephalo-)myopathies
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 16 (3. 1993), p. 534-536
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1993
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15
Smeitink, J., Ruitenbeek, W., ... Mitochondrial creatine kinase activity in patients with disturbed energy generation in muscle mitochondria
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 17 (1. 1994), p. 67-73
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1994
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16
Ruitenbeek, W., Wendel, U., ... Genetic counselling and prenatal diagnosis in disorders of the mitochondrial energy metabolism
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 19 (4. 1996), p. 581-587
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1996
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17
Smeitink, J., Loeffen, J., ... Molecular characterization and mutational analysis of the human B17 subunit of the mitochondrial respiratory chain complex I
in: Human genetics , ISSN 1432-1203, Vol. 103 (2. 1998), p. 245-250
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1998
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18
Ruitenbeek, M., Barbon, A., ... Evidence for a new type of vanadyl pairs in (VO)2P2O7: an ESR and magnetisation study
in: Catalysis letters , ISSN 1572-879X, Vol. 54 (3. 1998), p. 101-104
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1998
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19
Burlina, A. B., Gibson, K. M., ... Profound neurological phenotype in a patient presenting with disordered isoleucine and energy metabolism
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (8. 1998), p. 864-866
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1998
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20
Schulze, A., Mayatepek, E., ... In vivo methods useful for therapy monitoring in lactic acidosis
in: Journal of inherited metabolic disease , ISSN 1573-2665, ZDB-ID 2006875X Vol. 21 (6. 1998), p. 691-692
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1998