Zenker M - Search Results

1

Skeletal impairment in Pierson syndrome: Is there a role for lamininβ2 in bone physiology?

Beaufils C, Farlay D, Machuca-Gayet I, Fassier A, Zenker M, Freychet C, Bonnelye E, Bertholet-Thomas A, Ranchin B, Bacchetta J. Beaufils C, et al. Among authors: zenker m. Bone. 2018 Jan;106:187-193. doi: 10.1016/j.bone.2017.10.015. Epub 2017 Oct 16. Bone. 2018. PMID: 29051055

2

Prenatal findings in four consecutive pregnancies with fetal Pierson syndrome, a newly defined congenital nephrosis syndrome.

Mark K, Reis A, Zenker M. Mark K, et al. Among authors: zenker m. Prenat Diagn. 2006 Mar;26(3):262-6. doi: 10.1002/pd.1393. Prenat Diagn. 2006. PMID: 16450351

3

A syndrome comprising childhood-onset glomerular kidney disease and ocular abnormalities with progressive loss of vision is caused by mutated LAMB2.

Matejas V, Al-Gazali L, Amirlak I, Zenker M. Matejas V, et al. Among authors: zenker m. Nephrol Dial Transplant. 2006 Nov;21(11):3283-6. doi: 10.1093/ndt/gfl463. Epub 2006 Aug 18. Nephrol Dial Transplant. 2006. PMID: 16921188

4

Neurodevelopmental deficits in Pierson (microcoria-congenital nephrosis) syndrome.

Wühl E, Kogan J, Zurowska A, Matejas V, Vandevoorde RG, Aigner T, Wendler O, Lesniewska I, Bouvier R, Reis A, Weis J, Cochat P, Zenker M. Wühl E, et al. Among authors: zenker m. Am J Med Genet A. 2007 Feb 15;143(4):311-9. doi: 10.1002/ajmg.a.31564. Am J Med Genet A. 2007. PMID: 17256789

5

A milder variant of Pierson syndrome.

Kagan M, Cohen AH, Matejas V, Vlangos C, Zenker M. Kagan M, et al. Among authors: zenker m. Pediatr Nephrol. 2008 Feb;23(2):323-7. doi: 10.1007/s00467-007-0624-x. Epub 2007 Oct 18. Pediatr Nephrol. 2008. PMID: 17943323

6

Variable phenotype of Pierson syndrome.

Choi HJ, Lee BH, Kang JH, Jeong HJ, Moon KC, Ha IS, Yu YS, Matejas V, Zenker M, Choi Y, Cheong HI. Choi HJ, et al. Among authors: zenker m. Pediatr Nephrol. 2008 Jun;23(6):995-1000. doi: 10.1007/s00467-008-0748-7. Pediatr Nephrol. 2008. PMID: 18278520

7

Analysis of genes encoding laminin beta2 and related proteins in patients with Galloway-Mowat syndrome.

Dietrich A, Matejas V, Bitzan M, Hashmi S, Kiraly-Borri C, Lin SP, Mildenberger E, Hoppe B, Palm L, Shiihara T, Steiss JO, Tsai JD, Vester U, Weber S, Wühl E, Zepf K, Zenker M. Dietrich A, et al. Among authors: zenker m. Pediatr Nephrol. 2008 Oct;23(10):1779-86. doi: 10.1007/s00467-008-0880-4. Epub 2008 Jul 2. Pediatr Nephrol. 2008. PMID: 18594871

8

Ophthalmological aspects of Pierson syndrome.

Bredrup C, Matejas V, Barrow M, Bláhová K, Bockenhauer D, Fowler DJ, Gregson RM, Maruniak-Chudek I, Medeira A, Mendonça EL, Kagan M, Koenig J, Krastel H, Kroes HY, Saggar A, Sawyer T, Schittkowski M, Swietliński J, Thompson D, VanDeVoorde RG, Wittebol-Post D, Woodruff G, Zurowska A, Hennekam RC, Zenker M, Russell-Eggitt I. Bredrup C, et al. Among authors: zenker m. Am J Ophthalmol. 2008 Oct;146(4):602-611. doi: 10.1016/j.ajo.2008.05.039. Epub 2008 Jul 31. Am J Ophthalmol. 2008. PMID: 18672223

9

[Michel Pierson's syndrome].

Cochat P, Zenker M. Cochat P, et al. Among authors: zenker m. Arch Pediatr. 2011 Nov;18(11):1127-9. doi: 10.1016/j.arcped.2011.08.002. Epub 2011 Sep 7. Arch Pediatr. 2011. PMID: 21903364 French. No abstract available.

10

Paternal isodisomy of chromosome 3 unmasked by autosomal recessive microcoria-congenital nephrosis syndrome (Pierson syndrome) in a child with no other phenotypic abnormalities.

Matejas V, Muscheites J, Wigger M, Kreutzer HJ, Nizze H, Zenker M. Matejas V, et al. Among authors: zenker m. Am J Med Genet A. 2011 Oct;155A(10):2601-4. doi: 10.1002/ajmg.a.34214. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910237 No abstract available.

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