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

2. Genotype–Phenotype Association in ABCA4-Associated Retinopathy

7. Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders

9. Widespread subclinical cellular changes revealed across a neural-epithelial-vascular complex in choroideremia using adaptive optics

11. Analysis of Anatomic and Functional Measures in X-Linked Retinoschisis

12. Contributors

13. Intrathecal Gene Therapy for Giant Axonal Neuropathy

14. GM1 Gangliosidosis Type II: Results of a 10-Year Prospective Study

15. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

16. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

18. OUTER RETINAL MICROCAVITATIONS IN RETINITIS PIGMENTOSA

19. The qMini assay identifies an overlooked class of splice variants

21. Defining the clinical phenotype of Saul–Wilson syndrome

22. RPGR: Deep Phenotyping and Genetic Characterization With Findings Specific to the 3′-end of ORF15

23. Novel TMEM98, MFRP, PRSS56 variants in a large United States high hyperopia and nanophthalmos cohort

25. Neuropathy target esterase activity predicts retinopathy amongPNPLA6disorders

26. Chromosomal microarray analysis supplements exome sequencing to diagnose children with suspected inborn errors of immunity

27. Ophthalmic Manifestations of ROSAH (Retinal Dystrophy, Optic Nerve Edema, Splenomegaly, Anhidrosis, and Headache) Syndrome, an Inherited NF κB–Mediated Autoinflammatory Disease with Retinal Dystrophy

28. Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome.

29. Neuropathy target esterase activity predicts retinopathy among PNPLA6 disorders

32. Chromosomal Microarray Analysis Supplements Exome Sequencing to Diagnose Children with Suspected Inborn Errors of Immunity

33. Structural integrity of retinal pigment epithelial cells in eyes with age-related scattered hypofluorescent spots on late phase indocyanine green angiography (ASHS-LIA)

34. Photoreceptor and Retinal Pigment Epithelium Relationships in Eyes With Vitelliform Macular Dystrophy Revealed by Multimodal Adaptive Optics Imaging

35. Gain-of-function mutations inALPK1cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome

37. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

38. Novel ophthalmic findings and deep phenotyping in Williams-Beuren syndrome

40. Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies

42. Photoreceptor degeneration in ABCA4-associated retinopathy and its genetic correlates

43. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

44. Gain-of-function mutations in cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.

45. Whats new and important in pediatric ophthalmology and strabismus

47. Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

48. Correction to:An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

50. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

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