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51. Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5

55. Does Acculturation Matter?: Food Insecurity and Child Problem Behavior among Low-Income, Working Hispanic Households

56. Heterozygous and homozygous variants in STX1A cause a neurodevelopmental disorder with or without epilepsy

59. Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies

64. The Genetic Landscape of Complex Childhood‐Onset Hyperkinetic Movement Disorders

66. Factors Associated With Severe Illness in Patients Aged <21 Years Hospitalized for COVID-19

67. Novel DNM1L variants impair mitochondrial dynamics through divergent mechanisms

68. MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia

70. MED27, SLC6A7, and MPPE1 Variants in a Complex Neurodevelopmental Disorder with Severe Dystonia

72. Missense variants in the voltage sensing and pore domain of KCNH5 cause neurodevelopmental phenotypes including epilepsy

73. COVID-19 Patient Vaccine Program Design and Implementation

74. Performance Evaluation in Reference Services in ARL Libraries. SPEC Kit 139.

75. Use of the University of Minnesota's Walter Library: A Follow-Up Survey of Student Users.

76. Use of the University of Minnesota's Walter Library: A Survey of Student Users.

78. Synergistic use of glycomics and single‐molecule molecular inversion probes for identification of congenital disorders of glycosylation type‐1

79. The KCNB1 phenotypic and genetic spectrum

80. Determinants of School Performance in Guatemala: Family Background Characteristics and Early Abilities.

81. School Efficiency in Rural Guatemala.

85. Transitional care models in adolescent kidney transplant recipients—a systematic review.

95. 4-Aminopyridine is a promising treatment option for patients with gain-of-function KCNA2 -encephalopathy

96. Neurological involvement in children with hemolytic uremic syndrome

99. Loss‐of‐function variants in HOPS complex genes VPS16 and VPS41 cause early‐onset dystonia associated with lysosomal abnormalities

100. Publisher Correction:Whole-genome sequencing of a sporadic primary immunodeficiency cohort (Nature, (2020), 583, 7814, (90-95), 10.1038/s41586-020-2265-1)

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