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Höglund, Pia
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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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/..
 
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