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Schossig, Anna Sarah
20  results:
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1

Impaired epidermal barrier in autosomal recessive congenita..:

Seidl‐Philipp, Magdalena ; Schossig, Anna Sarah ; Moosbrugger‐Martinz, Verena...
JDDG: Journal der Deutschen Dermatologischen Gesellschaft.  17 (2019)  7 - p. 742-745 , 2019
Link: https://doi.org/10.1111/..
 
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2

Gestörte Hautbarriere bei zwei österreichischen Schwestern ..:

Seidl‐Philipp, Magdalena ; Schossig, Anna Sarah ; Moosbrugger‐Martinz, Verena...
JDDG: Journal der Deutschen Dermatologischen Gesellschaft.  17 (2019)  7 - p. 742-745 , 2019
Link: https://doi.org/10.1111/..
 
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3

Slow growth of hair and nails, craniofacial abnormalities a..:

Gruber, Robert ; Schossig, Anna Sarah ; Alnutaifi, Kholood A....
JDDG: Journal der Deutschen Dermatologischen Gesellschaft.  11 (2013)  10 - p. 1023-1025 , 2013
Link: https://doi.org/10.1111/..
 
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4

Vermindertes Haar‐ und Nagelwachstum, kraniofaziale Dysmorp..:

Gruber, Robert ; Schossig, Anna Sarah ; Alnutaifi, Kholood A....
JDDG: Journal der Deutschen Dermatologischen Gesellschaft.  11 (2013)  10 - p. 1023-1025 , 2013
Link: https://doi.org/10.1111/..
 
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5

Spektrum der Ichthyosen in einer österreichischen Ichthyose..:

Seidl‐Philipp, Magdalena ; Schatz, Ulrich A. ; Gasslitter, Irina...
JDDG: Journal der Deutschen Dermatologischen Gesellschaft.  18 (2020)  1 - p. 17-26 , 2020
Link: https://doi.org/10.1111/..
 
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6

Spectrum of ichthyoses in an Austrian ichthyosis cohort fro..:

Seidl‐Philipp, Magdalena ; Schatz, Ulrich A. ; Gasslitter, Irina...
JDDG: Journal der Deutschen Dermatologischen Gesellschaft.  18 (2019)  1 - p. 17-25 , 2019
Link: https://doi.org/10.1111/..
 
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7

Evidence of mild founderLMOD3mutations causing nemaline myo..:

Schatz, Ulrich A. ; Weiss, Simone ; Wenninger, Stephan...
Neurology.  91 (2018)  18 - p. , 2018
Link: https://doi.org/10.1212/..
 
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8

Cystatin M/E Variant Causes Autosomal Dominant Keratosis Fo..:

Eckl, Katja M. ; Gruber, Robert ; Brennan, Louise...
Frontiers in Genetics.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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9

Kohlschütter-Tönz Syndrome With a Novel ROGD1 Variant in 3 ..:

Akgün-Doğan, Özlem ; Simsek-Kiper, Pelin Ozlem ; Taşkıran, Ekim...
Journal of Child Neurology.  36 (2021)  10 - p. 816-822 , 2021
Link: https://doi.org/10.1177/..
 
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10

SYNE1-ataxia: Novel genotypic and phenotypic findings:

Indelicato, Elisabetta ; Nachbauer, Wolfgang ; Fauth, Christine...
Parkinsonism & Related Disorders.  62 (2019)  - p. 210-214 , 2019
Link: https://doi.org/10.1016/..
 
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11

Cleft lip/palate and hereditary diffuse gastric cancer: rep..:

Obermair, Florian ; Rammer, Melanie ; Burghofer, Jonathan...
Familial Cancer.  18 (2018)  2 - p. 253-260 , 2018
Link: https://doi.org/10.1007/..
 
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12

High risk of peri‐implant disease in periodontal Ehlers–Dan..:

Rinner, Alexander ; Zschocke, Johannes ; Schossig, Anna...
Clinical Oral Implants Research.  29 (2018)  11 - p. 1101-1106 , 2018
Link: https://doi.org/10.1111/..
 
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13

Variable expressivity of TCTEX1D2 mutations and a possible ..:

Zschocke, Johannes ; Schossig, Anna ; Bosshardt, Dieter D....
Archives of Oral Biology.  80 (2017)  - p. 222-228 , 2017
Link: https://doi.org/10.1016/..
 
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14

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations i..:

Kapferer-Seebacher, Ines ; Pepin, Melanie ; Werner, Roland...
The American Journal of Human Genetics.  99 (2016)  5 - p. 1005-1014 , 2016
Link: https://doi.org/10.1016/..
 
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15

Clinical, morphological, biochemical, imaging and outcome p..:

Huemer, Martina ; Karall, Daniela ; Schossig, Anna...
Journal of Inherited Metabolic Disease.  38 (2015)  5 - p. 905-914 , 2015
Link: https://doi.org/10.1007/..
 
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