The HEMS Medical Crew Survey

por Rasmussen, Kristen, Sollid, Stephen JM
Publicado 2015

Apples and oranges in HEMS – Do we know what we compare?

por Rasmussen, Kristen, Sollid, Stephen JM
Publicado 2015

A Climatology of Extreme Convective Storms in Tropical and Subtropical East Asia and Their Ingredients for Heavy Rainfall as Seen by TRMM

por Panasawatwong, Warittha, Rasmussen, Kristen L., Bell, Michael M.
Publicado 2022

The variable nature of convection in the tropics and subtropics: A legacy of 16 years of the Tropical Rainfall Measuring Mission satellite

por Houze, Robert A., Rasmussen, Kristen L., Zuluaga, Manuel D., Brodzik, Stella R.
Publicado 2015

Training and assessment of non-technical skills in Norwegian helicopter emergency services: a cross-sectional and longitudinal study

por Rasmussen, Kristen, Langdalen, Henrik, Sollid, Stephen J. M., Abrahamsen, Eirik Bjorheim, Sørskår, Leif Inge K., Bondevik, Gunnar Tschudi, Abrahamsen, Håkon B.
Publicado 2019

Germline activating MTOR mutation arising through gonadal mosaicism in two brothers with megalencephaly and neurodevelopmental abnormalities

por Mroske, Cameron, Rasmussen, Kristen, Shinde, Deepali N., Huether, Robert, Powis, Zoe, Lu, Hsiao-Mei, Baxter, Ruth M., McPherson, Elizabeth, Tang, Sha
Publicado 2015

Yield of Additional Genetic Testing after Chromosomal Microarray for Diagnosis of Neurodevelopmental Disability and Congenital Anomalies: a clinical practice resource of the Americ...

por Waggoner, Darrel, Wain, Karen E., Dubuc, Adrian M., Conlin, Laura, Hickey, Scott E., Lamb, Allen N, Lese Martin, Christa, Morton, Cynthia C., Rasmussen, Kristen, Schuette, Jane L, Schwartz, Stuart, Miller, David T.
Publicado 2018

Lack of evidence of WNT3A as a candidate gene for congenital vertebral malformations

por Ghebranious, Nader, Raggio, Cathleen L, Blank, Robert D, McPherson, Elizabeth, Burmester, James K, Ivacic, Lynn, Rasmussen, Kristen, Kislow, Jennifer, Glurich, Ingrid, Jacobsen, F Stig, Faciszewski, Thomas, Pauli, Richard M, Boachie-Adjei, Oheneba, Giampietro, Philip F
Publicado 2007

A second cohort of CHD3 patients expands the molecular mechanisms known to cause Snijders Blok-Campeau syndrome

por Drivas, Theodore G., Li, Dong, Nair, Divya, Alaimo, Joseph T., Alders, Mariëlle, Altmüller, Janine, Barakat, Tahsin Stefan, Bebin, E. Martina, Bertsch, Nicole L., Blackburn, Patrick R., Blesson, Alyssa, Bouman, Arjan M., Brockmann, Knut, Brunelle, Perrine, Burmeister, Margit, Cooper, Gregory M., Denecke, Jonas, Dieux-Coëslier, Anne, Dubbs, Holly, Ferrer, Alejandro, Gal, Danna, Bartik, Lauren E., Gunderson, Lauren B., Hasadsri, Linda, Jain, Mahim, Karimov, Catherine, Keena, Beth, Klee, Eric W., Kloth, Katja, Lace, Baiba, Macchiaiolo, Marina, Marcadier, Julien L., Milunsky, Jeff M., Napier, Melanie P., Ortiz-Gonzalez, Xilma R., Pichurin, Pavel N., Pinner, Jason, Powis, Zoe, Prasad, Chitra, Radio, Francesca Clementina, Rasmussen, Kristen J., Renaud, Deborah L., Rush, Eric T., Saunders, Carol, Selcen, Duygu, Seman, Ann R., Shinde, Deepali N., Smith, Erica D., Smol, Thomas, Snijders Blok, Lot, Stoler, Joan M., Tang, Sha, Tartaglia, Marco, Thompson, Michelle L., van de Kamp, Jiddeke M., Wang, Jingmin, Weise, Dagmar, Weiss, Karin, Woitschach, Rixa, Wollnik, Bernd, Yan, Huifang, Zackai, Elaine H., Zampino, Giuseppe, Campeau, Philippe, Bhoj, Elizabeth
Publicado 2020