Dame C - Search Results

1

Fatal congenital copper transport defect caused by a homozygous likely pathogenic variant of SLC31A1.

Dame C, Horn D, Schomburg L, Grünhagen J, Chillon TS, Tietze A, Vogt A, Bührer C. Dame C, et al. Clin Genet. 2023 May;103(5):585-589. doi: 10.1111/cge.14289. Epub 2022 Dec 28. Clin Genet. 2023. PMID: 36562171

2

Liver regeneration after partial hepatectomy: inconsistent results of expression screenings for human, mouse, and rat microRNAs.

Raschzok N, Sallmon H, Dame C, Sauer IM. Raschzok N, et al. Among authors: dame c. Am J Physiol Gastrointest Liver Physiol. 2012 Feb 15;302(4):G470-1. doi: 10.1152/ajpgi.00494.2011. Am J Physiol Gastrointest Liver Physiol. 2012. PMID: 22314890 Free article. No abstract available.

3

Perinatal management of fetal hemolytic disease due to Rh incompatibility combined with fetal alloimmune thrombocytopenia due to HPA-5b incompatibility.

Schild RL, Hoch J, Plath H, Geissen C, Fahnenstich H, Dame C, Hansmann M. Schild RL, et al. Among authors: dame c. Ultrasound Obstet Gynecol. 1999 Jul;14(1):64-7. doi: 10.1046/j.1469-0705.1999.14010064.x. Ultrasound Obstet Gynecol. 1999. PMID: 10461341 Free article.

4

Homozygous alpha-thalassaemia and hypospadias--common aetiology or incidental association? Long-term survival of Hb Bart's hydrops syndrome leads to new aspects for counselling of alpha-thalassaemic traits.

Dame C, Albers N, Hasan C, Bode U, Eigel A, Hansmann M, Brenner R, Bartmann P. Dame C, et al. Eur J Pediatr. 1999 Mar;158(3):217-20. doi: 10.1007/s004310051053. Eur J Pediatr. 1999. PMID: 10094442

5

Developmental biology of thrombopoietin in the human fetus and neonate.

Dame C. Dame C. Acta Paediatr Suppl. 2002;91(438):54-65. doi: 10.1111/j.1651-2227.2002.tb02900.x. Acta Paediatr Suppl. 2002. PMID: 12477265 Review.

6

Candidate gene involved in genital ontogeny in chromosome region 16p13.3.

Dame C, Albers N, Bartmann P. Dame C, et al. Am J Med Genet. 1999 Sep 17;86(3):302-3. Am J Med Genet. 1999. PMID: 10482886 No abstract available.

7

Erythropoietin acts as a trophic factor in neonatal rat intestine.

Juul SE, Ledbetter DJ, Joyce AE, Dame C, Christensen RD, Zhao Y, DeMarco V. Juul SE, et al. Among authors: dame c. Gut. 2001 Aug;49(2):182-9. doi: 10.1136/gut.49.2.182. Gut. 2001. PMID: 11454792 Free PMC article.

8

[Erythropoietin as a biochemical parameter for fetal hypoxia].

Fahnenstich H, Dame C, Alléra A, Rosskamp R, Kowalewski S. Fahnenstich H, et al. Among authors: dame c. Klin Padiatr. 1995 Nov-Dec;207(6):326-30. doi: 10.1055/s-2008-1046562. Klin Padiatr. 1995. PMID: 8569134 German.

9

Homozygous alpha-thalassemia associated with hypospadias: SEA-type deletion does not affect expression of the -14 gene and loss of the straight theta1-globin gene on 16p13.3 is compensated by its duplicate straight theta2 on chromosome 10.

Utsch B, Albers N, Dame C, Bartmann P, Lentze MJ, Ludwig M. Utsch B, et al. Among authors: dame c. Am J Med Genet. 2001 Jul 1;101(3):286-7. doi: 10.1002/ajmg.1344. Am J Med Genet. 2001. PMID: 11424149 No abstract available.

10

Cholesterol dynamics in the foetal and neonatal brain as reflected by circulatory levels of 24S-hydroxycholesterol.

Lütjohann D, Björkhem I, Locatelli S, Dame C, Schmolling J, von Bergmann K, Fahnenstich H. Lütjohann D, et al. Among authors: dame c. Acta Paediatr. 2001 Jun;90(6):652-7. doi: 10.1080/080352501750258720. Acta Paediatr. 2001. PMID: 11440099

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