Jacob K - Search Results

1

Beta 3-adrenergic-receptor allele distributions in children, adolescents and young adults with obesity, underweight or anorexia nervosa.

Hinney A, Lentes KU, Rosenkranz K, Barth N, Roth H, Ziegler A, Hennighausen K, Coners H, Wurmser H, Jacob K, Römer G, Winnikes U, Mayer H, Herzog W, Lehmkuhl G, Poustka F, Schmidt MH, Blum WF, Pirke KM, Schäfer H, Grzeschik KH, Remschmidt H, Hebebrand J. Hinney A, et al. Among authors: jacob k. Int J Obes Relat Metab Disord. 1997 Mar;21(3):224-30. doi: 10.1038/sj.ijo.0800391. Int J Obes Relat Metab Disord. 1997. PMID: 9080262

2

Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults.

Lentes KU, Hinney A, Ziegler A, Rosenkranz K, Wurmser H, Barth N, Jacob K, Coners H, Mayer H, Grzeschik KH, Schäfer H, Remschmidt H, Pirke KM, Hebebrand J. Lentes KU, et al. Among authors: jacob k. Life Sci. 1997;61(1):PL9-16. doi: 10.1016/s0024-3205(97)00361-5. Life Sci. 1997. PMID: 9200673

3

Resting metabolic rate in preadolescent girls at high risk of obesity.

Wurmser H, Laessle R, Jacob K, Langhard S, Uhl H, Angst A, Müller A, Pirke KM. Wurmser H, et al. Among authors: jacob k. Int J Obes Relat Metab Disord. 1998 Aug;22(8):793-9. doi: 10.1038/sj.ijo.0800662. Int J Obes Relat Metab Disord. 1998. PMID: 9725640

4

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

5

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

6

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

7

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

8

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.

9

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.

10

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.

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