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Items: 16

1.

Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.

Berkovic SF, Oliver KL, Canafoglia L, Krieger P, Damiano JA, Hildebrand MS, Morbin M, Vears DF, Sofia V, Giuliano L, Garavaglia B, Simonati A, Santorelli FM, Gambardella A, Labate A, Belcastro V, Castellotti B, Ozkara C, Zeman A, Rankin J, Mole SE, Aguglia U, Farrell M, Rajagopalan S, McDougall A, Brammah S, Andermann F, Andermann E, Dahl HM, Franceschetti S, Carpenter S.

Brain. 2019 Jan 1;142(1):59-69. doi: 10.1093/brain/awy297.

PMID:
30561534
2.

Beyond Activity Based Funding. An experiment in Denmark.

Burau V, Dahl HM, Jensen LG, Lou S.

Health Policy. 2018 Jul;122(7):714-721. doi: 10.1016/j.healthpol.2018.04.007. Epub 2018 Apr 24. Review.

PMID:
29724575
3.

Outpatient clinics treating substance use disorders in Northwest Russia and Northern Norway: a descriptive comparative study.

Dahl HM, Rezvyy G, Bogdanov A, Øiesvold T.

Int J Circumpolar Health. 2017;76(1):1411733. doi: 10.1080/22423982.2017.1411733.

4.

Neurofibromatosis type 2: Multiple intra-dermal tumors in a toddler.

Rustad CF, Dahl HM, Bowers NL, Sitek JC, Heiberg A, Huson S, Prescott T, Evans DGR.

Am J Med Genet A. 2017 May;173(5):1447-1449. doi: 10.1002/ajmg.a.38177. Epub 2017 Apr 3. No abstract available.

PMID:
28371307
5.

Navigating the field of temporally framed care in the Danish home care sector.

Tufte P, Dahl HM.

Sociol Health Illn. 2016 Jan;38(1):109-22. doi: 10.1111/1467-9566.12343. Epub 2015 Oct 16.

PMID:
26474802
6.

Young girl with psychosis, cognitive failure and seizures.

Slettedal IÖ, Dahl HM, Sandvig I, Dalmau J, Strømme P.

Tidsskr Nor Laegeforen. 2012 Oct 2;132(18):2073-6. doi: 10.4045/tidsskr.12.0092. English, Norwegian. No abstract available.

7.

Motivational interviewing for substance abuse.

Smedslund G, Berg RC, Hammerstrøm KT, Steiro A, Leiknes KA, Dahl HM, Karlsen K.

Cochrane Database Syst Rev. 2011 May 11;(5):CD008063. doi: 10.1002/14651858.CD008063.pub2. Review.

PMID:
21563163
8.

Unexpected myopathy associated with a mutation in MYBPC3 and misplacement of the cardiac myosin binding protein C.

Tajsharghi H, Leren TP, Abdul-Hussein S, Tulinius M, Brunvand L, Dahl HM, Oldfors A.

J Med Genet. 2010 Aug;47(8):575-7. doi: 10.1136/jmg.2009.072710. Epub 2009 Oct 26.

PMID:
19858127
9.

Advances in Molecular and Cellular Therapies for Hearing Loss.

Hildebrand MS, Newton SS, Gubbels SP, Sheffield AM, Kochhar A, de Silva MG, Dahl HM, Rose SD, Behlke MA, Smith RJ.

Mol Ther. 2008 Feb;16(2):224-236. doi: 10.1038/sj.mt.6300351. Epub 2016 Dec 7. Review.

PMID:
28178538
10.

[Tuberous sclerosis].

Dahl HM, Strømme P.

Tidsskr Nor Laegeforen. 2007 Mar 29;127(7):853. Norwegian. No abstract available.

11.

The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both?

Chinnery PF, Thorburn DR, Samuels DC, White SL, Dahl HM, Turnbull DM, Lightowlers RN, Howell N.

Trends Genet. 2000 Nov;16(11):500-5.

PMID:
11074292
12.

Cloning, mapping and expression analysis of the sheep Wilson disease gene homologue.

Lockhart PJ, Wilcox SA, Dahl HM, Mercer JF.

Biochim Biophys Acta. 2000 Apr 25;1491(1-3):229-39.

PMID:
10760584
13.

Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA.

White SL, Shanske S, Biros I, Warwick L, Dahl HM, Thorburn DR, Di Mauro S.

Prenat Diagn. 1999 Dec;19(12):1165-8.

PMID:
10590437
14.

Tooth root resorption associated with a familial bone dysplasia affecting mother and daughter.

Olsen CB, Tangchaitrong K, Chippendale I, Graham HK, Dahl HM, Stockigt JR.

Pediatr Dent. 1999 Sep-Oct;21(6):363-7. Review.

PMID:
10509339
15.

[Ascent of the testis].

Dahl HM, Nerhus TK, Haga OS, Haukaas S.

Tidsskr Nor Laegeforen. 1995 Feb 20;115(5):598-600. Norwegian.

PMID:
7900113
16.

The structure of a thirty-six kilobase region of the human chromosome including the fibroblast interferon gene IFN-beta.

Gross G, Mayr U, Bruns W, Grosveld F, Dahl HM, Collins J.

Nucleic Acids Res. 1981 Jun 11;9(11):2495-507.

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