Jacob K - Search Results

1

Interdependence between degree of porphyrin excess and disease severity in congenital erythropoietic porphyria (Günther's disease).

Freesemann AG, Bhutani LK, Jacob K, Doss MO. Freesemann AG, et al. Among authors: jacob k. Arch Dermatol Res. 1997 Apr;289(5):272-6. doi: 10.1007/s004030050192. Arch Dermatol Res. 1997. PMID: 9164637

2

Haem precursors and porphobilinogen deaminase in erythrocytes and lymphocytes of patients with acute intermittent porphyria.

Gross U, Jacob K, Frank M, Doss MO. Gross U, et al. Among authors: jacob k. Cell Mol Biol (Noisy-le-grand). 1997 Feb;43(1):29-35. Cell Mol Biol (Noisy-le-grand). 1997. PMID: 9074786

3

5-Aminolevulinic acid dehydratase deficiency porphyria: a twenty-year clinical and biochemical follow-up.

Gross U, Sassa S, Jacob K, Deybach JC, Nordmann Y, Frank M, Doss MO. Gross U, et al. Among authors: jacob k. Clin Chem. 1998 Sep;44(9):1892-6. Clin Chem. 1998. PMID: 9732973

4

Studies on coproporphyrin isomers in urine and feces in the porphyrias.

Kühnel A, Gross U, Jacob K, Doss MO. Kühnel A, et al. Among authors: jacob k. Clin Chim Acta. 1999 Apr;282(1-2):45-58. doi: 10.1016/s0009-8981(99)00036-4. Clin Chim Acta. 1999. PMID: 10340433

5

Composition of urinary coproporphyrin isomers I-IV in human porphyrias.

Jacob K, Doss MO. Jacob K, et al. Eur J Clin Chem Clin Biochem. 1993 Oct;31(10):617-24. doi: 10.1515/cclm.1993.31.10.617. Eur J Clin Chem Clin Biochem. 1993. PMID: 8292661

6

Excretion pattern of faecal coproporphyrin isomers I-IV in human porphyrias.

Jacob K, Doss MO. Jacob K, et al. Eur J Clin Chem Clin Biochem. 1995 Dec;33(12):893-901. doi: 10.1515/cclm.1995.33.12.893. Eur J Clin Chem Clin Biochem. 1995. PMID: 8845420 Clinical Trial.

7

Investigations on the formation of urinary coproporphyrin isomers I-IV in 5-aminolevulinic acid dehydratase deficiency porphyria, acute lead intoxication and after oral 5-aminolevulinic acid loading.

Jacob K, Egeler E, Gross U, Doss MO. Jacob K, et al. Clin Biochem. 1999 Mar;32(2):119-23. doi: 10.1016/s0009-9120(98)00104-0. Clin Biochem. 1999. PMID: 10211628 Clinical Trial.

8

Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.

Gross U, Puy H, Kühnel A, Meissauer U, Deybach JC, Jacob K, Martasek P, Nordmann Y, Doss MO. Gross U, et al. Among authors: jacob k. Cell Mol Biol (Noisy-le-grand). 2002 Feb;48(1):49-55. Cell Mol Biol (Noisy-le-grand). 2002. PMID: 11929047 Review.

9

Biochemical compared to molecular diagnosis in acute intermittent porphyria.

Grob U, Puy H, Jacob K, Deybach JC, Kremer J, Doss MO. Grob U, et al. Among authors: jacob k. J Inherit Metab Dis. 2006 Feb;29(1):157-61. doi: 10.1007/s10545-006-0155-9. J Inherit Metab Dis. 2006. PMID: 16601882

10

[Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria].

Doss MO, Gross U, Puy H, Doss M, Kühnel A, Jacob K, Deybach JC, Nordmann Y. Doss MO, et al. Among authors: jacob k. Med Klin (Munich). 2002 Jan 15;97(1):1-5. doi: 10.1007/s00063-002-1117-0. Med Klin (Munich). 2002. PMID: 11831056 German.

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