Schmitz J - Search Results

1

Congenital sucrase-isomaltase deficiency arising from cleavage and secretion of a mutant form of the enzyme.

Jacob R, Zimmer KP, Schmitz J, Naim HY. Jacob R, et al. Among authors: schmitz j. J Clin Invest. 2000 Jul;106(2):281-7. doi: 10.1172/JCI9677. J Clin Invest. 2000. PMID: 10903344 Free PMC article.

2

Sucrase-isomaltase deficiency in humans. Different mutations disrupt intracellular transport, processing, and function of an intestinal brush border enzyme.

Naim HY, Roth J, Sterchi EE, Lentze M, Milla P, Schmitz J, Hauri HP. Naim HY, et al. Among authors: schmitz j. J Clin Invest. 1988 Aug;82(2):667-79. doi: 10.1172/JCI113646. J Clin Invest. 1988. PMID: 3403721 Free PMC article.

3

Description of two different patients with abetalipoproteinemia: synthesis of a normal-sized apolipoprotein B-48 in intestinal organ culture.

Bouma ME, Beucler I, Pessah M, Heinzmann C, Lusis AJ, Naim HY, Ducastelle T, Leluyer B, Schmitz J, Infante R, et al. Bouma ME, et al. Among authors: schmitz j. J Lipid Res. 1990 Jan;31(1):1-15. J Lipid Res. 1990. PMID: 2179443 Free article.

4

Letter: Sucrase-isomaltase deficiency.

Schmitz J, Rey J, Hadorn B. Schmitz J, et al. N Engl J Med. 1976 Oct 14;295(16):902-3. doi: 10.1056/NEJM197610142951620. N Engl J Med. 1976. PMID: 958299 No abstract available.

5

Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two families.

Pessah M, Benlian P, Beucler I, Loux N, Schmitz J, Junien C, Infante R. Pessah M, et al. Among authors: schmitz j. J Clin Invest. 1991 Jan;87(1):367-70. doi: 10.1172/JCI114996. J Clin Invest. 1991. PMID: 1985110 Free PMC article.

6

Hypobetalipoproteinemia with accumulation of an apoprotein B-like protein in intestinal cells. Immunoenzymatic and biochemical characterization of seven cases of Anderson's disease.

Bouma ME, Beucler I, Aggerbeck LP, Infante R, Schmitz J. Bouma ME, et al. Among authors: schmitz j. J Clin Invest. 1986 Aug;78(2):398-410. doi: 10.1172/JCI112590. J Clin Invest. 1986. PMID: 2426307 Free PMC article.

7

Absence of brush border sucrase-isomaltase complex in congenital sucrose intolerance.

Schmitz J, Commegrain C, Maestracci D, Rey J. Schmitz J, et al. Biomedicine. 1974 Nov 20;21(11):440-3. Biomedicine. 1974. PMID: 4464992 No abstract available.

8

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy.

Rötig A, Cormier V, Blanche S, Bonnefont JP, Ledeist F, Romero N, Schmitz J, Rustin P, Fischer A, Saudubray JM, et al. Rötig A, et al. Among authors: schmitz j. J Clin Invest. 1990 Nov;86(5):1601-8. doi: 10.1172/JCI114881. J Clin Invest. 1990. PMID: 2243133 Free PMC article.

9

Specific expression of surface interferon-gamma on interferon-gamma producing T cells from mouse and man.

Assenmacher M, Scheffold A, Schmitz J, Segura Checa JA, Miltenyi S, Radbruch A. Assenmacher M, et al. Among authors: schmitz j. Eur J Immunol. 1996 Jan;26(1):263-7. doi: 10.1002/eji.1830260141. Eur J Immunol. 1996. PMID: 8566077

10

[Polyacrylamide gel electrophoresis analysis of membrane proteins of microvilli and of a cytoplasmic fraction in 8 cases of congenital saccharose intolerance].

Schmitz J, Bresson JL, Triadou N, Bataille J, Rey J. Schmitz J, et al. Gastroenterol Clin Biol. 1980 Apr;4(4):251-6. Gastroenterol Clin Biol. 1980. PMID: 7188272 French.

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