Ho ML - Search Results

1

Developmental brain abnormalities and acute encephalopathy in a patient with myopathy with extrapyramidal signs secondary to pathogenic variants in MICU1.

Wilton KM, Morales-Rosado JA, Selcen D, Muthusamy K, Ewing S, Agre K, Nickels K, Klee EW, Ho ML, Morava E. Wilton KM, et al. Among authors: ho ml. JIMD Rep. 2020 Mar 20;53(1):22-28. doi: 10.1002/jmd2.12114. eCollection 2020 May. JIMD Rep. 2020. PMID: 32395406 Free PMC article.

2

Novel Homozygous Variant in TTC19 Causing Mitochondrial Complex III Deficiency with Recurrent Stroke-Like Episodes: Expanding the Phenotype.

Conboy E, Selcen D, Brodsky M, Gavrilova R, Ho ML. Conboy E, et al. Among authors: ho ml. Semin Pediatr Neurol. 2018 Jul;26:16-20. doi: 10.1016/j.spen.2018.04.003. Semin Pediatr Neurol. 2018. PMID: 29961508

3

Serial prenatal and postnatal MRI of dystroglycanopathy in a patient with familial B3GALNT2 mutation.

Ho ML, Glenn OA, Sherr EH, Strober JB. Ho ML, et al. Pediatr Radiol. 2017 Jun;47(7):884-888. doi: 10.1007/s00247-017-3821-1. Epub 2017 Mar 16. Pediatr Radiol. 2017. PMID: 28303321

4

Bilateral Labyrinthine and Internal Auditory Canal Enhancement in an Infant With Severe Labyrinthine Dysplasia: A Previously Unreported Phenomenon.

Anzalone CL, Ho ML, Patel NS, Schimmenti LA, DeJong MD, Carlson ML. Anzalone CL, et al. Among authors: ho ml. Otol Neurotol. 2017 Jun;38(5):e21-e25. doi: 10.1097/MAO.0000000000001392. Otol Neurotol. 2017. PMID: 28346292

5

Prenatal or Perinatal Injury? Diagnosing the Cortically Blind Infant.

Ho ML, Mansukhani SA, Brodsky MC. Ho ML, et al. Am J Ophthalmol. 2020 Mar;211:56-62. doi: 10.1016/j.ajo.2019.10.026. Epub 2019 Nov 5. Am J Ophthalmol. 2020. PMID: 31704229

6

Arterial Spin Labeling Applications in Pediatric and Adult Neurologic Disorders.

Bambach S, Smith M, Morris PP, Campeau NG, Ho ML. Bambach S, et al. Among authors: ho ml. J Magn Reson Imaging. 2022 Mar;55(3):698-719. doi: 10.1002/jmri.27438. Epub 2020 Dec 11. J Magn Reson Imaging. 2022. PMID: 33314349 Review.

7

Novel truncating variant in KMT2E associated with cerebellar hypoplasia and velopharyngeal dysfunction.

Abreu NJ, Siemon AE, Baylis AL, Kirschner RE, Pfau RB, Ho ML, Hickey SE, Truxal KV. Abreu NJ, et al. Among authors: ho ml. Clin Case Rep. 2022 Feb 11;10(2):e05277. doi: 10.1002/ccr3.5277. eCollection 2022 Feb. Clin Case Rep. 2022. PMID: 35169466 Free PMC article.

8

Congenital Brain Malformations: An Integrated Diagnostic Approach.

Chaudhari BP, Ho ML. Chaudhari BP, et al. Among authors: ho ml. Semin Pediatr Neurol. 2022 Jul;42:100973. doi: 10.1016/j.spen.2022.100973. Epub 2022 Apr 22. Semin Pediatr Neurol. 2022. PMID: 35868725 Review.

9

Accelerated visual recovery from protracted hypoxic cortical blindness in a child.

Mansukhani S, Ho ML, Bradley EA, Brodsky MC. Mansukhani S, et al. Among authors: ho ml. Am J Ophthalmol Case Rep. 2019 Aug 2;16:100534. doi: 10.1016/j.ajoc.2019.100534. eCollection 2019 Dec. Am J Ophthalmol Case Rep. 2019. PMID: 31517136 Free PMC article.

10

Role of Electroencephalogram (EEG) and Magnetic Resonance Imaging (MRI) Findings in Early Recognition and Diagnosis of Neuronal Ceroid Lipofuscinosis Type 2 Disease.

Ho ML, Wirrell EC, Petropoulou K, Sakonju A, Chu D, Seratti G, Palasis S. Ho ML, et al. J Child Neurol. 2022 Dec;37(12-14):984-991. doi: 10.1177/08830738221128773. Epub 2022 Oct 3. J Child Neurol. 2022. PMID: 36184928

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