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Page 1
Single-Center Incidence and Patterns of Stroke in Early Renal Anhydramnios After Serial Amnioinfusions.
J Pediatr. 2024 Apr 12;271:114053. doi: 10.1016/j.jpeds.2024.114053. Online ahead of print.
J Pediatr. 2024.
PMID: 38615944
Case 1: A Case of Decreased Feeding and Lethargy in an 8-week-old Boy.
Byrd C, Lammert DB, Prochaska E, Cai S.
Byrd C, et al. Among authors: lammert db.
Pediatr Rev. 2024 Jun 1;45(6):329-332. doi: 10.1542/pir.2022-005910.
Pediatr Rev. 2024.
PMID: 38821898
No abstract available.
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Correspondence on "Recognition and Management of Delirium in the Neonatal Intensive Care Unit: Case Series From a Single-Center Level IV Intensive Care Unit".
Chavez-Valdez R, Northington FJ, Sharp A, Burton VJ, Lammert DB, Jantzie LL, Robinson S, Stafstrom CE, Ferriero D, Gano D, Numis A, Gerner G, Scafidi J, Gilmore M, Allen MC, Hilberg M, Parkinson C.
Chavez-Valdez R, et al. Among authors: lammert db.
J Child Neurol. 2024 May 31:8830738241259054. doi: 10.1177/08830738241259054. Online ahead of print.
J Child Neurol. 2024.
PMID: 38819375
No abstract available.
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Pearls & Oy-sters: Epilepsy Is a Key Feature of Pediatric-Onset Huntington Disease.
Lammert DB, Bang J, Stafstrom CE.
Lammert DB, et al.
Neurology. 2023 Nov 14;101(20):e2051-e2055. doi: 10.1212/WNL.0000000000207867. Epub 2023 Aug 31.
Neurology. 2023.
PMID: 37652706
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Fatal SARS-CoV-2 Inflammatory Syndrome and Myocarditis in an Adolescent: A Case Report.
Beaudry JT, Dietrick B, Lammert DB, Constas A, McCaw J, Hammond J, Buendia M, Stein JE, Pekosz A, Schuette J, Mostafa HH, Hooper JE, Bernier M, Agwu A, Feldman LS.
Beaudry JT, et al. Among authors: lammert db.
Pediatr Infect Dis J. 2021 Feb 1;40(2):e72-e76. doi: 10.1097/INF.0000000000002978.
Pediatr Infect Dis J. 2021.
PMID: 33181783
Free PMC article.
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Central and peripheral dysmyelination in a 3-year-old girl with ring chromosome 18.
Lammert DB, Miedema D, Ochotorena J, Dosa N, Petropoulou K, Lebel RR, Sakonju A.
Lammert DB, et al.
Clin Case Rep. 2019 Sep 27;7(11):2087-2091. doi: 10.1002/ccr3.2426. eCollection 2019 Nov.
Clin Case Rep. 2019.
PMID: 31788257
Free PMC article.
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The de novo autism spectrum disorder RELN R2290C mutation reduces Reelin secretion and increases protein disulfide isomerase expression.
Lammert DB, Middleton FA, Pan J, Olson EC, Howell BW.
Lammert DB, et al.
J Neurochem. 2017 Jul;142(1):89-102. doi: 10.1111/jnc.14045. Epub 2017 May 18.
J Neurochem. 2017.
PMID: 28419454
Free PMC article.
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RELN Mutations in Autism Spectrum Disorder.
Lammert DB, Howell BW.
Lammert DB, et al.
Front Cell Neurosci. 2016 Mar 31;10:84. doi: 10.3389/fncel.2016.00084. eCollection 2016.
Front Cell Neurosci. 2016.
PMID: 27064498
Free PMC article.
Review.
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