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Smigiel, R
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1

DOZ047.94: The thoracoscopic approach for esophageal atresi..:

Patkowski, D ; Gerus, S ; Rasiewicz, M...
Diseases of the Esophagus.  32 (2019)  Supplement_1 - p. , 2019
Link: https://doi.org/10.1093/..
 
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2

DOZ047.58: The familial occurrence of congenital esophageal..:

Smigiel, R ; Dzielendziak, A ; Toczewski, K...
Diseases of the Esophagus.  32 (2019)  Supplement_1 - p. , 2019
Link: https://doi.org/10.1093/..
 
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3

DOZ047.23: How esophageal atresia affects the family life:

Rozensztrauch, A ; Patkowski, D ; Śmigiel, R
Diseases of the Esophagus.  32 (2019)  Supplement_1 - p. , 2019
Link: https://doi.org/10.1093/..
 
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4

DOZ047.38: 10-years of experience with thoracoscopic approa..:

Dzielendziak, A ; Toczewski, K ; Śmigiel, R.
Diseases of the Esophagus.  32 (2019)  Supplement_1 - p. , 2019
Link: https://doi.org/10.1093/..
 
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5

New evidence for association of recessive IARS gene mutatio..:

Smigiel, R. ; Biela, M. ; Biernacka, A....
Clinical Genetics.  92 (2017)  6 - p. 671-673 , 2017
Link: https://doi.org/10.1111/..
 
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6

Is c.1431-12G>A A common European mutation of SPINK5? repor..:

Śmigiel, R ; Królak-Olejnik, B ; Śniegórska, D...
Balkan Journal of Medical Genetics.  19 (2016)  2 - p. 81-84 , 2016
Link: https://doi.org/10.1515/..
 
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7

Alternations in genes expression of pathway signaling in es..:

Smigiel, R. ; Lebioda, A. ; Blaszczyński, M....
Diseases of the Esophagus.  28 (2014)  3 - p. 229-233 , 2014
Link: https://doi.org/10.1111/..
 
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8

Normal exon copy number of theGLI2andGLI3genes in patients ..:

Bednarczyk, D. ; Smigiel, R. ; Patkowski, D....
Diseases of the Esophagus.  , 2013
Link: https://doi.org/10.1111/..
 
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9

Severe clinical course of Hirschsprung disease in a Mowat-W..:

Smigiel, R. ; Szafranska, A. ; Czyzewska, M....
Journal of Applied Genetics.  51 (2010)  1 - p. 111-113 , 2010
Link: https://doi.org/10.1007/..
 
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10

Use of Sliding-Window Fourier Transform in the Analysis of ..:

Smigiel, R. ; Knoll, A. ; Broll, N..
Materials Science Forum.  278-281 (1998)  - p. 170-176 , 1998
Link: https://doi.org/10.4028/..
 
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11

Neurodevelopmental disorder in a patient with HMBS and SCN3..:

M, Kłaniewska ; M, Rydzanicz ; J, Bladowska...
American Journal of Medical Genetics Part A.  194 (2024)  8 - p. , 2024
Link: https://doi.org/10.1002/..
 
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12

Metabolic Parameters in Patients with Prader-Willi Syndrome..:

Krefft M ; Frydecka D ; Śmigiel R.
https://www.dovepress.com/metabolic-parameters-in-patients-with-prader-willi-syndrome-and-digeor-peer-reviewed-article-NDT.  , 2020
Link: https://doaj.org/article..
 
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13

Mowat-Wilson syndrome : growth charts:

Ivanovski I ; Djuric O ; Broccoli S...
info:eu-repo/semantics/altIdentifier/pmid/32539836.  , 2020
Link: http://hdl.handle.net/24..
 
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14

Mowat-Wilson syndrome: growth charts:

Ivanovski I ; Djuric O ; Broccoli S...
info:eu-repo/semantics/altIdentifier/pmid/32539836.  , 2020
Link: http://hdl.handle.net/11..
 
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15

Mowat-Wilson syndrome: Growth charts:

Ivanovski I ; Djuric O ; Broccoli S...
info:eu-repo/semantics/altIdentifier/pmid/32539836.  , 2020
Link: http://hdl.handle.net/11..
 
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