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Alcohol use among Congolese Babembe male refugees in Tarrant County: A qualitative study

PloS one, 2022-08, Vol.17 (8), p.e0272293-e0272293

2022

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Long-Term Follow-Up of CD19-CAR T-Cell Therapy in Children and Young Adults With B-ALL

Journal of clinical oncology, 2021-05, Vol.39 (15), p.1650-1659

2021

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Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation

Genetics in medicine, 2017-02, Vol.19 (2), p.160-168

2017

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Measures, Metrics, and Indicators for Evaluating Technology-Based Interventions

International journal of human-computer interaction, 2023-07, Vol.39 (11), p.2199-2210

2023

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Research to Controversy in 10 Decades

Educational researcher, 2016-03, Vol.45 (2), p.122-133

Baker, Eva L.

2016

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Long-term follow-up after lymphodepleting autologous haematopoietic cell transplantation for treatment-resistant systemic lupus erythematosus

Rheumatology (Oxford, England), 2022-08, Vol.61 (8), p.3317-3328

2022

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Classification of learning outcomes: evidence from the computer games literature

Curriculum journal (London, England), 2005-12, Vol.16 (4), p.455-474

2005

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The Chimera of Validity

Teachers College record (1970), 2013-09, Vol.115 (9), p.1-26

Baker, Eva L

2013

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Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study

Lancet neurology, 2014-08, Vol.13 (8), p.777-787

2014

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Uptake of cancer screenings among a multiethnic refugee population in North Texas, 2014-2018

PloS one, 2020-03, Vol.15 (3), p.e0230675-e0230675

2020

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Neurofilament light chain levels correlate with clinical measures in CLN3 disease

Genetics in medicine, 2021-04, Vol.23 (4), p.751-757

2021

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Brain proton MR spectroscopy measurements in CLN3 disease

Molecular genetics and metabolism, 2023-05, Vol.139 (1), p.107584-107584, Article 107584

2023

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From the Assessment OF Education to the Assessment for Education: Policy and Futures

Teachers College record (1970), 2014-11, Vol.116 (11), p.1-24

Baker, Eva L

2014

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GM1 gangliosidosis type II: Results of a 10-year prospective study

Genetics in medicine, 2024-07, Vol.26 (7), p.101144, Article 101144

2024

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Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients

Molecular genetics and metabolism, 2023-02, Vol.138 (2), p.107508-107508, Article 107508

2023

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Neurocognitive phenotype of isolated methylmalonic acidemia

Pediatrics (Evanston), 2012-06, Vol.129 (6), p.e1541

2012

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Late diagnosis and atypical brain imaging of Aicardi–Goutières syndrome: are we failing to diagnose Aicardi–Goutières syndrome‐2?

Developmental medicine and child neurology, 2017-12, Vol.59 (12), p.1307-1311

2017

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Early Identification of Reading Difficulties Using Heterogeneous Developmental Trajectories

Journal of educational psychology, 2008-02, Vol.100 (1), p.192-208

2008

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Seizure phenotype in CLN3 disease and its relation to other neurologic outcome measures

Journal of inherited metabolic disease, 2021-07, Vol.44 (4), p.1013-1020

2021

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Neoadjuvant chemotherapy of locally advanced breast cancer: predicting response with in vivo (1)H MR spectroscopy--a pilot study at 4 T

Radiology, 2004-11, Vol.233 (2), p.424

2004

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Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors

Molecular genetics and metabolism, 2015-06, Vol.115 (2-3), p.128-140

2015

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The MEK inhibitor selumetinib reduces spinal neurofibroma burden in patients with NF1 and plexiform neurofibromas

Neuro-oncology advances, 2020-01, Vol.2 (1), p.vdaa095-vdaa095

2020

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Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis

American journal of medical genetics. Part A, 2016-10, Vol.170A (10), p.2605-2610

2016

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Alcohol use among Congolese Babembe male refugees in Tarrant County: A qualitative study

Long-Term Follow-Up of CD19-CAR T-Cell Therapy in Children and Young Adults With B-ALL

Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation

Measures, Metrics, and Indicators for Evaluating Technology-Based Interventions

Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants

Research to Controversy in 10 Decades

Long-term follow-up after lymphodepleting autologous haematopoietic cell transplantation for treatment-resistant systemic lupus erythematosus

Classification of learning outcomes: evidence from the computer games literature

The Chimera of Validity

Oral cysteamine bitartrate and N-acetylcysteine for patients with infantile neuronal ceroid lipofuscinosis: a pilot study

Uptake of cancer screenings among a multiethnic refugee population in North Texas, 2014-2018

Neurofilament light chain levels correlate with clinical measures in CLN3 disease

Brain proton MR spectroscopy measurements in CLN3 disease

From the Assessment OF Education to the Assessment for Education: Policy and Futures

GM1 gangliosidosis type II: Results of a 10-year prospective study

Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndrome

Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients

Neurocognitive phenotype of isolated methylmalonic acidemia

Late diagnosis and atypical brain imaging of Aicardi–Goutières syndrome: are we failing to diagnose Aicardi–Goutières syndrome‐2?

Early Identification of Reading Difficulties Using Heterogeneous Developmental Trajectories

Seizure phenotype in CLN3 disease and its relation to other neurologic outcome measures

Neoadjuvant chemotherapy of locally advanced breast cancer: predicting response with in vivo (1)H MR spectroscopy--a pilot study at 4 T

Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchors

The MEK inhibitor selumetinib reduces spinal neurofibroma burden in patients with NF1 and plexiform neurofibromas

Somatic AKT1 mutations cause meningiomas colocalizing with a characteristic pattern of cranial hyperostosis

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