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Items: 1 to 50 of 163

1.

Tobacco Marketing at SNAP- and WIC-Authorized Retail Food Stores in the United States.

Rust SM, Myers AE, D'Angelo H, Queen TL, Laska MN, Ribisl KM.

Health Educ Behav. 2019 Mar 2:1090198119831759. doi: 10.1177/1090198119831759. [Epub ahead of print]

PMID:
30829070
2.

A hospital-based study on caregiver preferences on acute seizure rescue medications in pediatric patients with epilepsy: Intranasal midazolam versus rectal diazepam.

Nunley S, Glynn P, Rust S, Vidaurre J, Albert DVF, Patel AD.

Epilepsy Behav. 2019 Jan 3;92:53-56. doi: 10.1016/j.yebeh.2018.12.007. [Epub ahead of print]

PMID:
30611934
3.

Survival of Mycobacterium bovis during forage ensiling.

Grooms DL, Bolin SR, Plastow JL, Lim A, Hattey J, Durst PT, Rust SR, Allen MS, Buskirk DD, Smith RW.

Am J Vet Res. 2019 Jan;80(1):87-94. doi: 10.2460/ajvr.80.1.87.

PMID:
30605026
4.

Lathosterolosis: A Relatively Mild Case with Cataracts and Learning Difficulties.

Anderson R, Rust S, Ashworth J, Clayton-Smith J, Taylor RL, Clayton PT, Morris AAM.

JIMD Rep. 2019;44:79-84. doi: 10.1007/8904_2018_127. Epub 2018 Aug 11.

5.

Comorbidities in Childhood Celiac Disease: A Phenome Wide Association Study Using the Electronic Health Record.

Prinzbach A, Moosavinasab S, Rust S, Boyle B, Barnard JA, Huang Y, Lin S.

J Pediatr Gastroenterol Nutr. 2018 Oct;67(4):488-493. doi: 10.1097/MPG.0000000000002020.

PMID:
29746339
6.

QIL1-dependent assembly of MICOS complex-lethal mutation in C19ORF70 resulting in liver disease and severe neurological retardation.

Gödiker J, Grüneberg M, DuChesne I, Reunert J, Rust S, Westermann C, Wada Y, Classen G, Langhans CD, Schlingmann KP, Rodenburg RJ, Pohlmann R, Marquardt T.

J Hum Genet. 2018 Jun;63(6):707-716. doi: 10.1038/s10038-018-0442-y. Epub 2018 Apr 4.

PMID:
29618761
7.

Parenting a Child with Phenylketonuria (PKU): an Interpretative Phenomenological Analysis (IPA) of the Experience of Parents.

Carpenter K, Wittkowski A, Hare DJ, Medford E, Rust S, Jones SA, Smith DM.

J Genet Couns. 2018 Sep;27(5):1074-1086. doi: 10.1007/s10897-018-0227-7. Epub 2018 Feb 21.

8.

Healthcare Utilization Characteristics for Intranasal Midazolam Versus Rectal Diazepam.

Nunley S, Glynn P, Rust S, Vidaurre J, Albert DVF, Patel AD.

J Child Neurol. 2018 Feb;33(2):158-163. doi: 10.1177/0883073817744696. Epub 2017 Dec 12.

PMID:
29233042
9.

Association of Serotonin Transporter Gene AluJb Methylation with Major Depression, Amygdala Responsiveness, 5-HTTLPR/rs25531 Polymorphism, and Stress.

Schneider I, Kugel H, Redlich R, Grotegerd D, Bürger C, Bürkner PC, Opel N, Dohm K, Zaremba D, Meinert S, Schröder N, Straßburg AM, Schwarte K, Schettler C, Ambrée O, Rust S, Domschke K, Arolt V, Heindel W, Baune BT, Zhang W, Dannlowski U, Hohoff C.

Neuropsychopharmacology. 2018 May;43(6):1308-1316. doi: 10.1038/npp.2017.273. Epub 2017 Nov 7.

PMID:
29114103
10.

When one disease is not enough: succinyl-CoA: 3-oxoacid coenzyme A transferase (SCOT) deficiency due to a novel mutation in OXCT1 in an infant with known phenylketonuria.

Schwade JN, Endmann M, Hofmann T, Rust S, Sass JO, Rutsch F.

J Pediatr Endocrinol Metab. 2017 Oct 26;30(10):1121-1124. doi: 10.1515/jpem-2017-0177.

PMID:
28820737
11.

Limitations of galactose therapy in phosphoglucomutase 1 deficiency.

Nolting K, Park JH, Tegtmeyer LC, Zühlsdorf A, Grüneberg M, Rust S, Reunert J, Du Chesne I, Debus V, Schulze-Bahr E, Baxter RC, Wada Y, Thiel C, van Schaftingen E, Fingerhut R, Marquardt T.

Mol Genet Metab Rep. 2017 Jul 31;13:33-40. doi: 10.1016/j.ymgmr.2017.07.010. eCollection 2017 Dec.

12.

Social Functioning and Behaviour in Mucopolysaccharidosis IH [Hurlers Syndrome].

Lehtonen A, Rust S, Jones S, Brown R, Hare D.

JIMD Rep. 2018;39:75-81. doi: 10.1007/8904_2017_47. Epub 2017 Jul 29.

13.

SLC39A8 deficiency: biochemical correction and major clinical improvement by manganese therapy.

Park JH, Hogrebe M, Fobker M, Brackmann R, Fiedler B, Reunert J, Rust S, Tsiakas K, Santer R, Grüneberg M, Marquardt T.

Genet Med. 2018 Feb;20(2):259-268. doi: 10.1038/gim.2017.106. Epub 2017 Jul 27.

PMID:
28749473
14.

Recommendations on clinical trial design for treatment of Mucopolysaccharidosis Type III.

Ghosh A, Shapiro E, Rust S, Delaney K, Parker S, Shaywitz AJ, Morte A, Bubb G, Cleary M, Bo T, Lavery C, Bigger BW, Jones SA.

Orphanet J Rare Dis. 2017 Jun 26;12(1):117. doi: 10.1186/s13023-017-0675-4.

15.

Phenotypic screening-the fast track to novel antibody discovery.

Minter RR, Sandercock AM, Rust SJ.

Drug Discov Today Technol. 2017 Mar;23:83-90. doi: 10.1016/j.ddtec.2017.03.004. Epub 2017 Apr 25. Review.

PMID:
28647091
16.

Relative size predicts competitive outcome through 2 million years.

Liow LH, Di Martino E, Krzeminska M, Ramsfjell M, Rust S, Taylor PD, Voje KL.

Ecol Lett. 2017 Aug;20(8):981-988. doi: 10.1111/ele.12795. Epub 2017 Jun 14.

PMID:
28614907
17.

Comparing the Genetic Diversity and Antimicrobial Resistance Profiles of Campylobacter jejuni Recovered from Cattle and Humans.

Cha W, Mosci RE, Wengert SL, Venegas Vargas C, Rust SR, Bartlett PC, Grooms DL, Manning SD.

Front Microbiol. 2017 May 9;8:818. doi: 10.3389/fmicb.2017.00818. eCollection 2017.

18.

Vineland adaptive behavior scales to identify neurodevelopmental problems in children with Congenital Hyperinsulinism (CHI).

Salomon-Estebanez M, Mohamed Z, Michaelidou M, Collins H, Rigby L, Skae M, Padidela R, Rust S, Dunne M, Cosgrove K, Banerjee I, Nicholson J.

Orphanet J Rare Dis. 2017 May 22;12(1):96. doi: 10.1186/s13023-017-0648-7.

19.

Cognitive endpoints for therapy development for neuronopathic mucopolysaccharidoses: Results of a consensus procedure.

van der Lee JH, Morton J, Adams HR, Clarke L, Ebbink BJ, Escolar ML, Giugliani R, Harmatz P, Hogan M, Jones S, Kearney S, Muenzer J, Rust S, Semrud-Clikeman M, Wijburg FA, Yu ZF, Janzen D, Shapiro E.

Mol Genet Metab. 2017 Jun;121(2):70-79. doi: 10.1016/j.ymgme.2017.05.004. Epub 2017 May 6.

20.

Simplified Readability Metric Drives Improvement of Radiology Reports: an Experiment on Ultrasound Reports at a Pediatric Hospital.

Chen W, Durkin C, Huang Y, Adler B, Rust S, Lin S.

J Digit Imaging. 2017 Dec;30(6):710-717. doi: 10.1007/s10278-017-9972-7.

21.

Venous Thromboembolism Prophylaxis in Postoperative Gynecologic Oncology Patients.

Over DR, Rust S, Fendley HF.

J Ark Med Soc. 2017 May;113(11):266-268. No abstract available.

PMID:
30351739
22.

Treatment Adherence and Psychological Wellbeing in Maternal Carers of Children with Phenylketonuria (PKU).

Medford E, Hare DJ, Carpenter K, Rust S, Jones S, Wittkowski A.

JIMD Rep. 2017;37:107-114. doi: 10.1007/8904_2017_23. Epub 2017 Apr 6.

23.

A Mutation in the G-Protein Gene GNB2 Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction.

Stallmeyer B, Kuß J, Kotthoff S, Zumhagen S, Vowinkel K, Rinné S, Matschke LA, Friedrich C, Schulze-Bahr E, Rust S, Seebohm G, Decher N, Schulze-Bahr E.

Circ Res. 2017 May 12;120(10):e33-e44. doi: 10.1161/CIRCRESAHA.116.310112. Epub 2017 Feb 20.

PMID:
28219978
24.

Patient-centered design criteria for wearable seizure detection devices.

Patel AD, Moss R, Rust SW, Patterson J, Strouse R, Gedela S, Haines J, Lin SM.

Epilepsy Behav. 2016 Nov;64(Pt A):116-121. doi: 10.1016/j.yebeh.2016.09.012. Epub 2016 Oct 12.

PMID:
27741462
25.

Phenotypic screening reveals TNFR2 as a promising target for cancer immunotherapy.

Williams GS, Mistry B, Guillard S, Ulrichsen JC, Sandercock AM, Wang J, González-Muñoz A, Parmentier J, Black C, Soden J, Freeth J, Jovanović J, Leyland R, Al-Lamki RS, Leishman AJ, Rust SJ, Stewart R, Jermutus L, Bradley JR, Bedian V, Valge-Archer V, Minter R, Wilkinson RW.

Oncotarget. 2016 Oct 18;7(42):68278-68291. doi: 10.18632/oncotarget.11943.

26.

Interspecific interactions through 2 million years: are competitive outcomes predictable?

Liow LH, Di Martino E, Voje KL, Rust S, Taylor PD.

Proc Biol Sci. 2016 Aug 31;283(1837). pii: 20160981. doi: 10.1098/rspb.2016.0981.

27.

Building Global Capacity for Conducting Operational Research Using the SORT IT Model: Where and Who?

Zachariah R, Rust S, Berger SD, Guillerm N, Bissell K, Delaunois P, Reid AJ, Kumar AM, Olliaro PL, Reeder JC, Harries AD, Ramsay A.

PLoS One. 2016 Aug 9;11(8):e0160837. doi: 10.1371/journal.pone.0160837. eCollection 2016.

28.

Distinctly Elevated Chitotriosidase Activity in a Child with Congenital Andersen Disease (Glycogen Storage Disease Type IV).

Schänzer A, Faas D, Rust S, Podskarbi T, van Kuilenburg AB, Scarpa M, Kunze A, Marquardt T, Hahn A.

Klin Padiatr. 2016 Sep;228(5):277-9. doi: 10.1055/s-0042-109399. Epub 2016 Jul 21. No abstract available.

PMID:
27442143
29.

Factors Associated with Shiga Toxin-Producing Escherichia coli Shedding by Dairy and Beef Cattle.

Venegas-Vargas C, Henderson S, Khare A, Mosci RE, Lehnert JD, Singh P, Ouellette LM, Norby B, Funk JA, Rust S, Bartlett PC, Grooms D, Manning SD.

Appl Environ Microbiol. 2016 Jul 29;82(16):5049-56. doi: 10.1128/AEM.00829-16. Print 2016 Aug 15.

30.

A phase 1/2 study of intrathecal heparan-N-sulfatase in patients with mucopolysaccharidosis IIIA.

Jones SA, Breen C, Heap F, Rust S, de Ruijter J, Tump E, Marchal JP, Pan L, Qiu Y, Chung JK, Nair N, Haslett PA, Barbier AJ, Wijburg FA.

Mol Genet Metab. 2016 Jul;118(3):198-205. doi: 10.1016/j.ymgme.2016.05.006. Epub 2016 May 10.

31.

Rapid Diagnosis of 83 Patients with Niemann Pick Type C Disease and Related Cholesterol Transport Disorders by Cholestantriol Screening.

Reunert J, Fobker M, Kannenberg F, Du Chesne I, Plate M, Wellhausen J, Rust S, Marquardt T.

EBioMedicine. 2015 Dec 22;4:170-5. doi: 10.1016/j.ebiom.2015.12.018. eCollection 2016 Feb.

32.

Development and validation of a spontaneous preterm delivery predictor in asymptomatic women.

Saade GR, Boggess KA, Sullivan SA, Markenson GR, Iams JD, Coonrod DV, Pereira LM, Esplin MS, Cousins LM, Lam GK, Hoffman MK, Severinsen RD, Pugmire T, Flick JS, Fox AC, Lueth AJ, Rust SR, Mazzola E, Hsu C, Dufford MT, Bradford CL, Ichetovkin IE, Fleischer TC, Polpitiya AD, Critchfield GC, Kearney PE, Boniface JJ, Hickok DE.

Am J Obstet Gynecol. 2016 May;214(5):633.e1-633.e24. doi: 10.1016/j.ajog.2016.02.001. Epub 2016 Feb 11.

33.

CCDC115 Deficiency Causes a Disorder of Golgi Homeostasis with Abnormal Protein Glycosylation.

Jansen JC, Cirak S, van Scherpenzeel M, Timal S, Reunert J, Rust S, Pérez B, Vicogne D, Krawitz P, Wada Y, Ashikov A, Pérez-Cerdá C, Medrano C, Arnoldy A, Hoischen A, Huijben K, Steenbergen G, Quelhas D, Diogo L, Rymen D, Jaeken J, Guffon N, Cheillan D, van den Heuvel LP, Maeda Y, Kaiser O, Schara U, Gerner P, van den Boogert MA, Holleboom AG, Nassogne MC, Sokal E, Salomon J, van den Bogaart G, Drenth JP, Huynen MA, Veltman JA, Wevers RA, Morava E, Matthijs G, Foulquier F, Marquardt T, Lefeber DJ.

Am J Hum Genet. 2016 Feb 4;98(2):310-21. doi: 10.1016/j.ajhg.2015.12.010. Epub 2016 Jan 28.

34.

SLC39A8 Deficiency: A Disorder of Manganese Transport and Glycosylation.

Park JH, Hogrebe M, Grüneberg M, DuChesne I, von der Heiden AL, Reunert J, Schlingmann KP, Boycott KM, Beaulieu CL, Mhanni AA, Innes AM, Hörtnagel K, Biskup S, Gleixner EM, Kurlemann G, Fiedler B, Omran H, Rutsch F, Wada Y, Tsiakas K, Santer R, Nebert DW, Rust S, Marquardt T.

Am J Hum Genet. 2015 Dec 3;97(6):894-903. doi: 10.1016/j.ajhg.2015.11.003.

35.

Ebola, fragile health systems and tuberculosis care: a call for pre-emptive action and operational research.

Zachariah R, Ortuno N, Hermans V, Desalegn W, Rust S, Reid AJ, Boeree MJ, Harries AD.

Int J Tuberc Lung Dis. 2015 Nov;19(11):1271-5. doi: 10.5588/ijtld.15.0355.

PMID:
26467577
36.

Phenotypic screening: the future of antibody discovery.

Gonzalez-Munoz AL, Minter RR, Rust SJ.

Drug Discov Today. 2016 Jan;21(1):150-156. doi: 10.1016/j.drudis.2015.09.014. Epub 2015 Oct 9. Review.

PMID:
26440132
37.

It Is Not Always Alcohol Abuse--A Transferrin Variant Impairing the CDT Test.

Zühlsdorf A, Said M, Seger C, Park JH, Reunert J, Rust S, Wada Y, Grüneberg M, DuChesne I, Marquardt T.

Alcohol Alcohol. 2016 Mar;51(2):148-53. doi: 10.1093/alcalc/agv099. Epub 2015 Sep 1.

PMID:
26333807
38.

News on Clinical Details and Treatment in PGM1-CDG.

Schrapers E, Tegtmeyer LC, Simic-Schleicher G, Debus V, Reunert J, Balbach S, Klingel K, Du Chesne I, Seelhöfer A, Fobker M, Marquardt T, Rust S.

JIMD Rep. 2016;26:77-84. doi: 10.1007/8904_2015_471. Epub 2015 Aug 25.

39.

TMEM165 Deficiency: Postnatal Changes in Glycosylation.

Schulte Althoff S, Grüneberg M, Reunert J, Park JH, Rust S, Mühlhausen C, Wada Y, Santer R, Marquardt T.

JIMD Rep. 2016;26:21-9. doi: 10.1007/8904_2015_455. Epub 2015 Aug 4.

40.

Identification of anti-tumour biologics using primary tumour models, 3-D phenotypic screening and image-based multi-parametric profiling.

Sandercock AM, Rust S, Guillard S, Sachsenmeier KF, Holoweckyj N, Hay C, Flynn M, Huang Q, Yan K, Herpers B, Price LS, Soden J, Freeth J, Jermutus L, Hollingsworth R, Minter R.

Mol Cancer. 2015 Jul 31;14:147. doi: 10.1186/s12943-015-0415-0.

41.

Autosomal-Recessive Mutations in SLC34A1 Encoding Sodium-Phosphate Cotransporter 2A Cause Idiopathic Infantile Hypercalcemia.

Schlingmann KP, Ruminska J, Kaufmann M, Dursun I, Patti M, Kranz B, Pronicka E, Ciara E, Akcay T, Bulus D, Cornelissen EA, Gawlik A, Sikora P, Patzer L, Galiano M, Boyadzhiev V, Dumic M, Vivante A, Kleta R, Dekel B, Levtchenko E, Bindels RJ, Rust S, Forster IC, Hernando N, Jones G, Wagner CA, Konrad M.

J Am Soc Nephrol. 2016 Feb;27(2):604-14. doi: 10.1681/ASN.2014101025. Epub 2015 Jun 5.

42.

Congenital nephrotic syndrome with dysmorphic features and death in early infancy: Answers.

Park JH, Weissensteiner M, Wagner O, Wada Y, Rust S, Reunert J, Marquardt T.

Pediatr Nephrol. 2016 Aug;31(8):1283-6. doi: 10.1007/s00467-015-3070-1. Epub 2015 May 9. No abstract available.

PMID:
25956699
43.

Congenital nephrotic syndrome with dysmorphic features and death in early infancy: Questions.

Park JH, Weissensteiner M, Wagner O, Wada Y, Rust S, Reunert J, Marquardt T.

Pediatr Nephrol. 2016 Aug;31(8):1281. doi: 10.1007/s00467-015-3071-0. Epub 2015 May 7. No abstract available.

PMID:
25947087
44.

A new case of UDP-galactose transporter deficiency (SLC35A2-CDG): molecular basis, clinical phenotype, and therapeutic approach.

Dörre K, Olczak M, Wada Y, Sosicka P, Grüneberg M, Reunert J, Kurlemann G, Fiedler B, Biskup S, Hörtnagel K, Rust S, Marquardt T.

J Inherit Metab Dis. 2015 Sep;38(5):931-40. doi: 10.1007/s10545-015-9828-6. Epub 2015 Mar 17.

PMID:
25778940
45.

Transferrin variants: pitfalls in the diagnostics of Congenital disorders of glycosylation.

Zühlsdorf A, Park JH, Wada Y, Rust S, Reunert J, DuChesne I, Grüneberg M, Marquardt T.

Clin Biochem. 2015 Jan;48(1-2):11-3. doi: 10.1016/j.clinbiochem.2014.09.022. Epub 2014 Oct 8.

PMID:
25305627
46.

Substances used and prevalence rates of pharmacological cognitive enhancement among healthy subjects.

Franke AG, Bagusat C, Rust S, Engel A, Lieb K.

Eur Arch Psychiatry Clin Neurosci. 2014 Nov;264 Suppl 1:S83-90. doi: 10.1007/s00406-014-0537-1. Epub 2014 Sep 12. Review.

PMID:
25214391
47.

Effects of tail docking on health and performance of beef cattle in confined, slatted-floor feedlots.

Kroll LK, Grooms DL, Siegford JM, Schweihofer JP, Metz K, Rust SR.

J Anim Sci. 2014 Sep;92(9):4108-14. doi: 10.2527/jas.2014-7582. Epub 2014 Jul 1.

PMID:
24987071
48.

The novel transferrin E592A variant impairs the diagnostics of congenital disorders of glycosylation.

Park JH, Zühlsdorf A, Wada Y, Roll C, Rust S, Du Chesne I, Grüneberg M, Reunert J, Marquardt T.

Clin Chim Acta. 2014 Sep 25;436:135-9. doi: 10.1016/j.cca.2014.05.011. Epub 2014 May 26. Erratum in: Clin Chim Acta. 2015 Jul 20;447:115-7.

PMID:
24875750
49.

Serotonin transporter gene methylation is associated with hippocampal gray matter volume.

Dannlowski U, Kugel H, Redlich R, Halik A, Schneider I, Opel N, Grotegerd D, Schwarte K, Schettler C, Ambrée O, Rust S, Domschke K, Arolt V, Heindel W, Baune BT, Suslow T, Zhang W, Hohoff C.

Hum Brain Mapp. 2014 Nov;35(11):5356-67. doi: 10.1002/hbm.22555. Epub 2014 May 23.

PMID:
24862560
50.

Multiple phenotypes in phosphoglucomutase 1 deficiency.

Marquardt T, Morava E, Rust S.

N Engl J Med. 2014 May 22;370(21):2051-2. doi: 10.1056/NEJMc1403446. No abstract available.

PMID:
24849093

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