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Items: 4

1.

A rare CFTR mutation associated with severe disease progression in a 10-year-old Hispanic patient.

Soe K, Gregoire-Bottex MM.

Clin Case Rep. 2017 Jan 19;5(2):139-144. doi: 10.1002/ccr3.764. eCollection 2017 Feb.

2.

Gastrointestinal dysfunction and autism: caution with misdiagnoses as many mysteries remain to be unraveled!

Greydanus DE, Gregoire-Bottex MM, Merrick J.

Int J Adolesc Med Health. 2016 Dec 15;29(6). pii: /j/ijamh.2017.29.issue-6/ijamh-2016-0127/ijamh-2016-0127.xml. doi: 10.1515/ijamh-2016-0127. No abstract available.

PMID:
27977400
3.

Improving the Rate of Sufficient Sweat Collected in Infants Referred for Sweat Testing in Michigan.

Abdulhamid I, Kleyn M, Langbo C, Gregoire-Bottex M, Schuen J, Shanmugasundaram K, Nasr SZ.

Glob Pediatr Health. 2014 Oct 9;1:2333794X14553625. doi: 10.1177/2333794X14553625. eCollection 2014.

4.

Evaluation of genetic counseling among cystic fibrosis carriers, Michigan Newborn Screening.

Kleyn MJ, Langbo C, Abdulhamid I, Adamski CR, Allan C, Carmany EP, Gregoire-Bottex MM, Homnick D, Schuen J, Nasr SZ.

Pediatr Pulmonol. 2013 Feb;48(2):123-9. doi: 10.1002/ppul.22703. Epub 2012 Nov 20.

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