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Brian Kirmse
Titolo
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Anno
The incidence of urea cycle disorders
ML Summar, S Koelker, D Freedenberg, C Le Mons, J Haberle, HS Lee, ...
Molecular genetics and metabolism 110 (1-2), 179-180, 2013
3132013
Newborn screening and early biochemical follow-up in combined methylmalonic aciduria and homocystinuria, cblC type, and utility of methionine as a secondary screening analyte
JD Weisfeld-Adams, MA Morrissey, BM Kirmse, BR Salveson, ...
Molecular genetics and metabolism 99 (2), 116-123, 2010
1302010
Study of LPIN1, LPIN2 and LPIN3 in rhabdomyolysis and exercise-induced myalgia
C Michot, L Hubert, NB Romero, A Gouda, A Mamoune, S Mathew, E Kirk, ...
Journal of inherited metabolic disease 35, 1119-1128, 2012
1092012
Factors Associated with Positive SARS-CoV-2 Test Results in Outpatient Health Facilities and Emergency Departments Among Children and Adolescents Aged 18 Years—Mississippi …
CV Hobbs
MMWR. Morbidity and Mortality Weekly Report 69, 2020
972020
High prevalence of structural heart disease in children with cblC-type methylmalonic aciduria and homocystinuria
LE Profitlich, B Kirmse, MP Wasserstein, GA Diaz, S Srivastava
Molecular genetics and metabolism 98 (4), 344-348, 2009
772009
HIV Protease Inhibitors Inhibit the Development of Preerythrocytic-Stage Plasmodium Parasites
CV Hobbs, T Voza, A Coppi, B Kirmse, K Marsh, W Borkowsky, P Sinnis
The Journal of infectious diseases 199 (1), 134-141, 2009
702009
Novel first-dose adverse drug reactions during a phase I trial of olipudase alfa (recombinant human acid sphingomyelinase) in adults with Niemann–Pick disease type B (acid …
MM McGovern, MP Wasserstein, B Kirmse, WL Duvall, T Schiano, ...
Genetics in Medicine 18 (1), 34-40, 2016
572016
Complex care of individuals with multiple sulfatase deficiency: Clinical cases and consensus statement
R Ahrens-Nicklas, L Schlotawa, A Ballabio, N Brunetti-Pierri, M De Castro, ...
Molecular genetics and metabolism 123 (3), 337-346, 2018
382018
CDC COVID-19 Response Team. Factors associated with positive SARS-CoV-2 test results in outpatient health facilities and emergency departments among children and adolescents …
CV Hobbs, LM Martin, SS Kim, BM Kirmse, L Haynie, S McGraw, P Byers, ...
MMWR Morb Mortal Wkly Rep 69 (50), 1925-1929, 2020
372020
Lower mitochondrial DNA and altered mitochondrial fuel metabolism in HIV-exposed uninfected infants in Cameroon
J Jao, KM Powis, B Kirmse, C Yu, F Epie, E Nshom, EJ Abrams, ...
Aids 31 (18), 2475-2481, 2017
352017
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation
W Khayat, A Hackett, M Shaw, A Ilie, T Dudding-Byth, VM Kalscheuer, ...
Human molecular genetics 28 (4), 598-614, 2019
312019
Loss of function mutations in GEMIN5 cause a neurodevelopmental disorder
S Kour, DS Rajan, TR Fortuna, EN Anderson, C Ward, Y Lee, S Lee, ...
Nature communications 12 (1), 2558, 2021
282021
Lower preprandial insulin and altered fuel use in HIV/antiretroviral-exposed infants in Cameroon
J Jao, B Kirmse, C Yu, Y Qiu, K Powis, E Nshom, F Epie, PM Tih, ...
The Journal of Clinical Endocrinology & Metabolism 100 (9), 3260-3269, 2015
272015
European registry and network for intoxication type metabolic diseases (E-IMD)
ML Summar, S Koelker, D Freedenberg, C Le Mons, J Haberle, HS Lee, ...
Electronic address: http://www. e-imd. org/en/index. phtml. Members of the …, 2013
272013
Genome sequencing as a first-line diagnostic test for hospitalized infants
KM Bowling, ML Thompson, CR Finnila, SM Hiatt, DR Latner, MD Amaral, ...
Genetics in Medicine 24 (4), 851-861, 2022
262022
COVID-19 in children: a review and parallels to other hyperinflammatory syndromes
CV Hobbs, A Khaitan, BM Kirmse, W Borkowsky
Frontiers in Pediatrics 8, 593455, 2020
262020
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila
LD Goodman, H Cope, Z Nil, TA Ravenscroft, WL Charng, S Lu, AC Tien, ...
The American Journal of Human Genetics 108 (9), 1669-1691, 2021
232021
Abnormal newborn screens and acylcarnitines in HIV-exposed and ARV-exposed infants
B Kirmse, CV Hobbs, I Peter, B LaPlante, M Caggana, K Kloke, ...
The Pediatric infectious disease journal 32 (2), 146-150, 2013
222013
Case report: ocular toxocariasis: a report of three cases from the Mississippi Delta
K Inagaki, B Kirmse, RS Bradbury, RS Moorthy, I Arguello, CD McGuffey, ...
The American Journal of Tropical Medicine and Hygiene 100 (5), 1223, 2019
172019
Acylcarnitine profiles in HIV-exposed, uninfected neonates in the United States
B Kirmse, TJ Yao, S Hofherr, D Kacanek, PL Williams, CV Hobbs, R Hazra, ...
AIDS Research and Human Retroviruses 32 (4), 339-348, 2016
152016
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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