Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Julie E Niemela

Showing results (1-10 of 55) with videos related to

Pageof 6
Sort By:
Current Opinion in Allergy and Clinical Immunology|October 21, 2009
Mutation analysis in primary immunodeficiency diseases: case studiesAmy P Hsu, Thomas A Fleisher, Julie E Niemela
Clinical Immunology (Orlando, Fla.)|July 26, 2002
CYBB mutation analysis in X-linked chronic granulomatous diseaseOrathai Jirapongsananuruk, Julie E Niemela, Harry L Malech, et al.
Frontiers in Immunology|November 19, 2014
Targeted NGS: A Cost-Effective Approach to Molecular Diagnosis of PIDsJennifer L Stoddard, Julie E Niemela, Thomas A Fleisher, et al.
Molecular and Cellular Probes|November 8, 2005
Single nucleotide polymorphisms in the apoptosis receptor gene TNFRSF6Julie E Niemela, Amy P Hsu, Thomas A Fleisher, et al.
Biological Psychiatry|October 4, 2005
Magnesium (mg) retention and mood effects after intravenous mg infusion in premenstrual dysphoric disorderKhursheed Khine, Donald L Rosenstein, Ronald J Elin, et al.
Journal of Clinical Immunology|May 8, 2015
Late-onset severe chronic active EBV in a patient for five years with mutations in STXBP2 (MUNC18-2) and PRF1 (perforin 1)Jeffrey I Cohen, Julie E Niemela, Jennifer L Stoddard, et al.
Pediatrics|October 9, 2013
Autoimmune lymphoproliferative syndrome misdiagnosed as hemophagocytic lymphohistiocytosisAmanda Rudman Spergel, Kelly Walkovich, Susan Price, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 15, 2011
FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndromeHye Sun Kuehn, Iusta Caminha, Julie E Niemela, et al.
The Journal of Allergy and Clinical Immunology|February 18, 2003
Diagnostic paradigm for evaluation of male patients with chronic granulomatous disease, based on the dihydrorhodamine 123 assayOrathai Jirapongsananuruk, Harry L Malech, Douglas B Kuhns, et al.
Asian Pacific Journal of Allergy and Immunology|April 25, 2012
Cryptococcal osteomyelitis in a child with a novel compound mutation of the IL12RB1 geneOrathai Jirapongsananuruk, Voravich Luangwedchakarn, Julie E Niemela, et al.
Pageof 6

Showing results (1-10 of 55) with videos related to

Sort By:
Pageof 6
Current Opinion in Allergy and Clinical Immunology|October 21, 2009
Mutation analysis in primary immunodeficiency diseases: case studiesAmy P Hsu, Thomas A Fleisher, Julie E Niemela
Clinical Immunology (Orlando, Fla.)|July 26, 2002
CYBB mutation analysis in X-linked chronic granulomatous diseaseOrathai Jirapongsananuruk, Julie E Niemela, Harry L Malech, et al.
Frontiers in Immunology|November 19, 2014
Targeted NGS: A Cost-Effective Approach to Molecular Diagnosis of PIDsJennifer L Stoddard, Julie E Niemela, Thomas A Fleisher, et al.
Molecular and Cellular Probes|November 8, 2005
Single nucleotide polymorphisms in the apoptosis receptor gene TNFRSF6Julie E Niemela, Amy P Hsu, Thomas A Fleisher, et al.
Biological Psychiatry|October 4, 2005
Magnesium (mg) retention and mood effects after intravenous mg infusion in premenstrual dysphoric disorderKhursheed Khine, Donald L Rosenstein, Ronald J Elin, et al.
Journal of Clinical Immunology|May 8, 2015
Late-onset severe chronic active EBV in a patient for five years with mutations in STXBP2 (MUNC18-2) and PRF1 (perforin 1)Jeffrey I Cohen, Julie E Niemela, Jennifer L Stoddard, et al.
Pediatrics|October 9, 2013
Autoimmune lymphoproliferative syndrome misdiagnosed as hemophagocytic lymphohistiocytosisAmanda Rudman Spergel, Kelly Walkovich, Susan Price, et al.
Journal of Immunology (Baltimore, Md. : 1950)|April 15, 2011
FAS haploinsufficiency is a common disease mechanism in the human autoimmune lymphoproliferative syndromeHye Sun Kuehn, Iusta Caminha, Julie E Niemela, et al.
The Journal of Allergy and Clinical Immunology|February 18, 2003
Diagnostic paradigm for evaluation of male patients with chronic granulomatous disease, based on the dihydrorhodamine 123 assayOrathai Jirapongsananuruk, Harry L Malech, Douglas B Kuhns, et al.
Asian Pacific Journal of Allergy and Immunology|April 25, 2012
Cryptococcal osteomyelitis in a child with a novel compound mutation of the IL12RB1 geneOrathai Jirapongsananuruk, Voravich Luangwedchakarn, Julie E Niemela, et al.
Pageof 6