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Showing 1 to 12 of 49 entries
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Correction for Pedersen et al., Regulation of CARD11 Signaling and Lymphoma Cell Survival by the E3 Ubiquitin Ligase RNF181.

Molecular and cellular biology

Pedersen SM, Chan W, Jattani RP, Mackie dS, Pomerantz JL.
PMID: 27034408
Mol Cell Biol. 2016 Mar 31;36(8):1322. doi: 10.1128/MCB.00106-16. Print 2016 Apr.

No abstract available.

A novel .

Journal of experimental and integrative medicine

Kurt B, Naini AB, Copeland WC, Lu J, Dimauro S, Hirano M.
PMID: 24265579
J Exp Integr Med. 2012;2(2). doi: 10.5455/jeim.200312.cr.001.

The human mitochondrial genome is replicated by DNA polymerase γ, which is encoded by polymerase γ gene (

ARN25068, a versatile starting point towards triple GSK-3β/FYN/DYRK1A inhibitors to tackle tau-related neurological disorders.

European journal of medicinal chemistry

Demuro S, Sauvey C, Tripathi SK, Di Martino RMC, Shi D, Ortega JA, Russo D, Balboni B, Giabbai B, Storici P, Girotto S, Abagyan R, Cavalli A.
PMID: 34959172
Eur J Med Chem. 2021 Dec 16;229:114054. doi: 10.1016/j.ejmech.2021.114054. Epub 2021 Dec 16.

The human kinome plays a crucial role in several pathways. Its dysregulation has been linked to diverse central nervous system (CNS)-related disorders with a drastic impact on the aging population. Among them, tauopathies, such as Alzheimer's Disease (AD) and...

Patient and Neurologist Preferences in the United States for Relapsing-Remitting Multiple Sclerosis Treatments: Findings from a Discrete Choice Experiment.

Patient preference and adherence

Kumar J, Cambron-Mellott MJ, Tencer T, Will O, Mackie DS, Beusterien K.
PMID: 34267507
Patient Prefer Adherence. 2021 Jul 08;15:1515-1527. doi: 10.2147/PPA.S306498. eCollection 2021.

BACKGROUND AND OBJECTIVE: Relapsing-remitting multiple sclerosis (RRMS) is a chronic inflammatory disease associated with central nervous system dysfunction and accelerated brain volume loss (BVL). There exists a paucity of research examining the importance of BVL to patients and neurologists...

The General Movements Assessment in Neonates With Hypoxic Ischemic Encephalopathy.

Journal of child neurology

Pouppirt NR, Martin V, Pagnotto-Hammitt L, Spittle AJ, Flibotte J, DeMauro SB.
PMID: 33439066
J Child Neurol. 2021 Jul;36(8):601-609. doi: 10.1177/0883073820981515. Epub 2021 Jan 13.

BACKGROUND: Clinical measures after birth and studies such as electroencephalogram (EEG) and brain imaging do not fully predict neurodevelopmental outcomes of infants with hypoxic-ischemic encephalopathy. Early detection of adverse neurologic outcomes, and cerebral palsy in particular, in high-risk infants...

ARN25068, a versatile starting point towards triple GSK-3β/FYN/DYRK1A inhibitors to tackle tau-related neurological disorders.

European journal of medicinal chemistry

Demuro S, Sauvey C, Tripathi SK, Di Martino RMC, Shi D, Ortega JA, Russo D, Balboni B, Giabbai B, Storici P, Girotto S, Abagyan R, Cavalli A.
PMID: 34959172
Eur J Med Chem. 2021 Dec 16;229:114054. doi: 10.1016/j.ejmech.2021.114054. Epub 2021 Dec 16.

The human kinome plays a crucial role in several pathways. Its dysregulation has been linked to diverse central nervous system (CNS)-related disorders with a drastic impact on the aging population. Among them, tauopathies, such as Alzheimer's Disease (AD) and...

Is it time to study routine car seat tolerance screening in a randomized controlled trial? An international survey of current practice and clinician equipoise.

Journal of perinatology : official journal of the California Perinatal Association

Jensen EA, Greenspan JS, Aghai ZH, Carola DL, Eichenwald EC, DeMauro SB, Dysart K.
PMID: 34453111
J Perinatol. 2021 Aug 27; doi: 10.1038/s41372-021-01167-7. Epub 2021 Aug 27.

No abstract available.

Duration of noninvasive respiratory support and risk for bronchopulmonary dysplasia or death.

Journal of perinatology : official journal of the California Perinatal Association

Gentle SJ, Carper B, Laughon MM, Jensen EA, Williams A, Travers CP, Ambalavanan N, Lal CV, Carlo WA, Polin RA, Laptook AR, Keszler M, Hensman AM, Vieira E, Little E, Pierre LS, Walsh MC, Hibbs AM, Newman NS, Truog WE, Pallotto EK, Kilbride HW, Gauldin C, Holmes A, Johnson K, Parimi PS, Gaetano L, Poindexter BB, Schibler K, Merhar SL, Alexander B, Grisby C, Kirker K, Cotten CM, Goldberg RN, Finkle J, Fisher KA, Bose CL, Bernhardt J, Bose G, Clark C, Kicklighter SD, Rhodes-Ryan G, White D, Carlton DP, Stoll BJ, Patel RM, Loggins Y, Hale EC, Bottcher DI, Mackie C, Bremer AA, Higgins RD, Archer SW, Sokol GM, Herron DE, Joyce J, Tyson JE, Khan AM, Kennedy KA, Eason E, Stephens EK, McDavid GE, Arldt-McAlister J, Burson K, Garcia C, Hall D, Martin K, Martin SC, Rodgers S, Tate PLP, Wright SL, Sánchez PJ, Nelin LD, Jadcherla SR, Luzader P, Clark E, Fortney CA, Gutentag J, Park C, Shadd JC, Stein M, Grothause JL, Baugher H, Yosseff-Salameh L, McCool J, Das A, Gantz MG, Bann CM, Wallace D, Crawford M, Gabrio J, Leblond D, O'Donnell Auman J, Huitema CMP, Zaterka-Baxter KM, Van Meurs KP, Chock VY, Stevenson DK, Ball MB, Proud MS, Reichert EN, Williams RJ, Collins MV, Cosby SS, McNair T, Estes M, Hagood K, Devaskar U, Garg M, Chanlaw T, Geller R, Bell EF, Colaizy TT, Baack ML, Ellsbury DL, Brumbaugh JE, Johnson KJ, Henning MM, Elenkiwich C, Goeke CA, Broadbent M, Hogden LA, Klein JM, Dagle JM, Schmelzel ML, Walker JR, Bass DB, Tud TL, Watterberg KL, Fuller J, Ohls RK, Lacy CB, Beauman SS, Hartenberger C, Hanson M, Kuan E, Eichenwald EC, Schmidt B, Kirpalani H, DeMauro SB, Abbasi S, Catts C, Chaudhary AS, Ghavam S, Mancini T, Snyder J, D'Angio CT, Guillet R, Reynolds AM, Lakshminrusimha S, Kent A, Binion K, Bowman M, Donato J, Guilford S, Hunn J, Jensen RL, Li E, Maffett D, Orme C, Prinzing D, Reubens L, Rochez D, Rowan M, Sabaratnam P, Sacilowski M, Scorsone AM, Wadkins HIM, Williams A, Wynn K, Jones R, Wyckoff M, Sánchez PJ, Brion LP, Vasil DM, Chen L, DeLeon MM, Eubanks F, Pavageau L, Sepulveda P, Yoder BA, Baserga M, Minton SD, Sheffield MJ, Rau CA, Burnett J, Davis B, Christensen S, Loertscher MC, Marchant T, Maxson E, McGrath K, Elmont JO, Parry M, Schaefer ST, Weaver-Lewis K, Woodbury KD, Shankaran S, Natarajan G, Chawla S, Sood BG, Childs K, Panaitescu B, Bara R, Barks J, Christensen MK, Wiggins SA, White DF.
PMID: 35034096
J Perinatol. 2022 Jan 15; doi: 10.1038/s41372-021-01269-2. Epub 2022 Jan 15.

OBJECTIVE: To determine whether the duration of noninvasive respiratory support exposure is associated with bronchopulmonary dysplasia (BPD) or death in preterm infants.METHODS: Multicenter, retrospective study of infants born at

Relationships between retinopathy of prematurity without ophthalmologic intervention and neurodevelopment and vision at 2 years.

Pediatric research

Brumbaugh JE, Bell EF, Hirsch SC, Crenshaw EG, DeMauro SB, Adams-Chapman IS, Lowe JR, Natarajan G, Wyckoff MH, Vohr BR, Colaizy TT, Harmon HM, Watterberg KL, Hintz SR.
PMID: 34686832
Pediatr Res. 2021 Oct 22; doi: 10.1038/s41390-021-01778-y. Epub 2021 Oct 22.

BACKGROUND: Severe retinopathy of prematurity (ROP) is associated with adverse outcomes. Relationships between milder ROP and outcomes have not been defined. We hypothesized that children with ROP stage ≤3 who did not receive ophthalmologic intervention would have worse motor,...

Disorders of carbohydrate metabolism.

Handbook of clinical neurology

Dimauro S, Akman O, Hays AP.
PMID: 18808999
Handb Clin Neurol. 2007;86:167-82. doi: 10.1016/S0072-9752(07)86007-6.

No abstract available.

A De Novo Mutation in .

Child neurology open

Kurt YG, Çoku J, Akman HO, Naini A, Lu J, Engelstad K, Hirano M, De Vivo DC, DiMauro S.
PMID: 28503604
Child Neurol Open. 2016 Apr 04;3:2329048X15627937. doi: 10.1177/2329048X15627937. eCollection 2016.

Dystonia is often associated with the symmetrical basal ganglia lesions of Leigh syndrome. However, it has also been associated with mitochondrial

Reliability of the Telemedicine Application of the Gross Motor Function Measure-88 in Patients With Leukodystrophy.

Pediatric neurology

Gavazzi F, Adang L, Waldman A, Jan AK, Liu G, Lorch SA, DeMauro SB, Shults J, Pierce SR, Ballance E, Kornafel T, Harrington A, Glanzman AM, Vanderver A.
PMID: 34624609
Pediatr Neurol. 2021 Dec;125:34-39. doi: 10.1016/j.pediatrneurol.2021.09.012. Epub 2021 Sep 24.

BACKGROUND: Leukodystrophies are a rare class of disorders characterized by severe neuromotor disability. There is a strong need for research regarding the functional status of people with leukodystrophy which is limited by the need for in-person assessments of mobility....

Showing 1 to 12 of 49 entries