Leupold D - Search Results

1

3-methyl-3-butenoic acid: an artefact in the urinary metabolic pattern of patients with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency.

Jakobs C, Bojasch M, Duran M, Ketting D, Wadman SK, Leupold D. Jakobs C, et al. Among authors: leupold d. Clin Chim Acta. 1980 Sep 8;106(1):85-9. doi: 10.1016/0009-8981(80)90377-0. Clin Chim Acta. 1980. PMID: 6157502 No abstract available.

2

CT findings in a case of deficiency of 3-hydroxy-3-methylglutaryl-CoA-lyase.

Lisson G, Leupold D, Bechinger D, Wallesch C. Lisson G, et al. Among authors: leupold d. Neuroradiology. 1981;22(2):99-101. doi: 10.1007/BF00344781. Neuroradiology. 1981. PMID: 6170906

3

3-hydroxy-3-methylglutaryl-CoA lyase deficiency in an infant with macrocephaly and mild metabolic acidosis.

Leupold D, Bojasch M, Jakobs C. Leupold D, et al. Eur J Pediatr. 1982 Feb;138(1):73-6. doi: 10.1007/BF00442334. Eur J Pediatr. 1982. PMID: 7075630

4

Urinary p-tyramine excretion in hypertyrosinaemia.

Bremer H, Jaenicke U, Leupold D. Bremer H, et al. Among authors: leupold d. Clin Chim Acta. 1969 Jan;23(1):244-6. doi: 10.1016/0009-8981(69)90034-5. Clin Chim Acta. 1969. PMID: 5812491 No abstract available.

5

Amino acid excretion of premature infants receiving different amounts of protein.

Przyrembel H, Leupold D, Tosberg P, Bremer HJ. Przyrembel H, et al. Among authors: leupold d. Clin Chim Acta. 1973 Nov 23;49(1):27-39. doi: 10.1016/0009-8981(73)90339-2. Clin Chim Acta. 1973. PMID: 4797173 No abstract available.

6

Clinical features and diagnostic approach in type I tyrosinaemia in an infant with cytomegaly virus infection and bacterial sepsis.

Wabitsch M, Pohlandt F, Leupold D, Berger R, Mönch E, Heinze E, Teller W. Wabitsch M, et al. Among authors: leupold d. Eur J Pediatr. 1993 Apr;152(4):327-30. doi: 10.1007/BF01956746. Eur J Pediatr. 1993. PMID: 8387006

7

Congenital pancreatic lipase deficiency.

Figarella C, De Caro A, Leupold D, Poley JR. Figarella C, et al. Among authors: leupold d. J Pediatr. 1980 Mar;96(3 Pt 1):412-6. doi: 10.1016/s0022-3476(80)80683-4. J Pediatr. 1980. PMID: 6153713

8

Atypical phenylketonuria with "dihydrobiopterin synthetase" deficiency: absence of phosphate-eliminating enzyme activity demonstrated in liver.

Niederwieser A, Leimbacher W, Curtius HC, Ponzone A, Rey F, Leupold D. Niederwieser A, et al. Among authors: leupold d. Eur J Pediatr. 1985 May;144(1):13-6. doi: 10.1007/BF00491917. Eur J Pediatr. 1985. PMID: 2990933

9

Molecular analysis and long-term follow-up of patients with different forms of 6-pyruvoyl-tetrahydropterin synthase deficiency.

Dudesek A, Röschinger W, Muntau AC, Seidel J, Leupold D, Thöny B, Blau N. Dudesek A, et al. Among authors: leupold d. Eur J Pediatr. 2001 May;160(5):267-76. doi: 10.1007/s004310000722. Eur J Pediatr. 2001. PMID: 11388593

10

Peritoneal dialysis in the treatment of metabolic crises caused by inherited disorders of organic and amino acid metabolism.

Gortner L, Leupold D, Pohlandt F, Bartmann P. Gortner L, et al. Among authors: leupold d. Acta Paediatr Scand. 1989 Sep;78(5):706-11. doi: 10.1111/j.1651-2227.1989.tb11130.x. Acta Paediatr Scand. 1989. PMID: 2596277

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