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Höglund, Pia
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Online (50)
Mediatypes
Articles (Online) (28)
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1
A missense mutation in SLC26A3 is associated with human mal..:
Wedenoja, Satu
;
Khamaysi, Ahlam
;
Shimshilashvili, Liana
...
Scientific Reports. 7 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1038/..
?
2
Follow‐up of a child with congenital chloride diarrhoea cau..:
Dechant, Markus‐Johann
;
Wedenoja, Satu
;
Höglund, Pia
...
Acta Paediatrica. 101 (2012) 6 - p. , 2012
Link:
https://doi.org/10.1111/..
?
3
Cl− Is Required for HCO3− Entry Necessary for Sperm Capacit..:
Chen, Wen Ying
;
Xu, Wen Ming
;
Chen, Zhang Hui
...
Biology of Reproduction. 80 (2009) 1 - p. 115-123 , 2009
Link:
https://doi.org/10.1095/..
?
4
Four novel mutations in the lactase gene (LCT) underlying c..:
Torniainen, Suvi
;
Freddara, Roberta
;
Routi, Taina
...
BMC Gastroenterology. 9 (2009) 1 - p. , 2009
Link:
https://doi.org/10.1186/..
?
5
Long‐Term Clinical Outcome in Patients With Congenital Chlo..:
Hihnala, Satu
;
Höglund, Pia
;
Lammi, Laura
...
Journal of Pediatric Gastroenterology and Nutrition. 42 (2006) 4 - p. 369-375 , 2006
Link:
https://doi.org/10.1097/..
?
6
Disruption of the SLC26A3-mediated anion transport is assoc..:
Höglund, Pia
;
Hihnala, Satu
;
Kujala, Minna
...
Fertility and Sterility. 85 (2006) 1 - p. 232-235 , 2006
Link:
https://doi.org/10.1016/..
?
7
Phenotypic consequences of genetic variation at hemizygous ..:
Kurotaki, Naohiro
;
Shen, Joseph J.
;
Touyama, Mayumi
...
Genetics in Medicine. 7 (2005) 7 - p. 479-483 , 2005
Link:
https://doi.org/10.1097/..
?
8
Interstitial 1q25.3‐q31.3 deletion in a boy with mild manif..:
Höglund, Pia
;
Jalkanen, Reetta
;
Marttinen, Eino
.
American Journal of Medical Genetics Part A. 123A (2003) 3 - p. 290-295 , 2003
Link:
https://doi.org/10.1002/..
?
9
Maternal and Paternal Chromosomes 7 Show Differential Methy..:
Hannula, Katariina
;
Lipsanen-Nyman, Marita
;
Scherer, Stephen W.
...
Genomics. 73 (2001) 1 - p. 1-9 , 2001
Link:
https://doi.org/10.1006/..
?
10
The congenital chloride diarrhea gene is expressed in semin..:
Haila, Siru
;
Saarialho-Kere, Ulpu
;
Karjalainen-Lindsberg, Marja-Liisa
...
Histochemistry and Cell Biology. 113 (2000) 4 - p. 279-286 , 2000
Link:
https://doi.org/10.1007/..
?
11
Molecular characterization of deletion at 11q22.1‐23.3 in m..:
Monni, Outi
;
Zhu, Ying
;
Franssila, Kaarle
...
British Journal of Haematology. 104 (1999) 4 - p. 665-671 , 1999
Link:
https://doi.org/10.1046/..
?
12
Genomic structure of the human congenital chloride diarrhea..:
Haila, Siru
;
Höglund, Pia
;
Scherer, Stephen W
...
Gene. 214 (1998) 1-2 - p. 87-93 , 1998
Link:
https://doi.org/10.1016/..
?
13
A serine/threonine kinase gene defective in Peutz–Jeghers s..:
Hemminki, Akseli
;
Markie, David
;
Tomlinson, Ian
...
Nature. 391 (1998) 6663 - p. 184-187 , 1998
Link:
https://doi.org/10.1038/..
?
14
Monoallelic Expression of HumanPEG1/MESTIs Paralleled by Pa..:
Riesewijk, Anne M.
;
Hu, Landian
;
Schulz, Ute
...
Genomics. 42 (1997) 2 - p. 236-244 , 1997
Link:
https://doi.org/10.1006/..
?
15
MUTATION SPECTRUM OF DRA IN CONGENITAL CHLORIDE DIARRHEA:
Höglund, Pia
;
Socha, Jerzy
;
Popinska, Kataryna
...
Journal of Pediatric Gastroenterology & Nutrition. 24 (1997) 4 - p. 472 , 1997
Link:
https://doi.org/10.1097/..
1-15