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Autor/in
- Gal, Andreas
- Beck, Michael 8
- Hübner, Christian 5
- Kampmann, Christoph 5
- Kurth, Ingo 5
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60 Einträge gefunden
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IgA nephropathy in two adolescent sisters heterozygous for Fabry disease.
- Whybra, Catharina
- Schwarting, Andreas
- Kriegsmann, Jörg
- Gal, Andreas
- Mengel, Eugen
- Kampmann, Christoph
- Baehner, Frank
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A new type of leukoencephalopathy with metaphyseal chondrodysplasia maps to Xq25-q27.
2006 - Forschungsinformationssystem des UKE -
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Disease manifestations and X inactivation in heterozygous females with Fabry disease.
- Maier, Esther M
- Osterrieder, Stephanie
- Whybra, Catharina
- Ries, Markus
- Gal, Andreas
- Beck, Michael
- Roscher, Adelbert A
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Pediatric Fabry disease.
- Ries, Markus
- Gupta, Surya
- Moore, David F
- Sachdev, Vandana
- Quirk, Jane M
- Murray, Gary J
- Rosing, Douglas R
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Renal failure and hypertension in Alagille syndrome with a novel JAG1 mutation.
- Harendza, Sigrid
- Hübner, Christian A
- Gläser, Christiane
- Burdelski, Martin
- Thaiss, Friedrich
- Hansmann, Ingo
- Gal, Andreas
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A novel 9 bp deletion in the filamin a gene causes an otopalatodigital-spectrum disorder with a variable, intermediate phenotype.
2005 - Forschungsinformationssystem des UKE -
Anemia is a new complication in Fabry disease: data from the Fabry Outcome Survey.
- Kleinert, Julia
- Dehout, François
- Schwarting, Andreas
- Lorenzo, de
- García, Abelardo
- Ricci, Roberta
- Kampmann, Christoph
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Protocadherin-21 (PCDH21), a candidate gene for human retinal dystrophies.
2005 - Forschungsinformationssystem des UKE - frei zugänglich -
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Seventeen novel PLP1 mutations in patients with Pelizaeus-Merzbacher disease.
- Hübner, Christian A
- Orth, Ulrike
- Senning, Arne
- Steglich, Cordula
- Kohlschütter, Alfried
- Korinthenberg, Rudolf
- Gal, Andreas
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Mild Pelizaeus-Merzbacher disease caused by a point mutation affecting correct splicing of PLP1 mRNA.
2005 - Forschungsinformationssystem des UKE -
Mucopolysaccharidosis type II in females: case report and review of literature.
2005 - Forschungsinformationssystem des UKE -
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Hyperchylomicronaemia due to lipoprotein lipase deficiency as a cause of false-positive newborn screening for biotinidase deficiency.
2005 - Forschungsinformationssystem des UKE -
Impaired calmodulin binding of myosin-7A causes autosomal dominant hearing loss (DFNA11).
- Bolz, Hanno
- Bolz, Steffen-Sebastian
- Götz, Schade
- Kothe, Christian
- Mohrmann, Gerrit
- Hess, Markus
- Gal, Andreas
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