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I.H. Maumenee
Observed name:
I H Maumenee
Institution:
Johns Hopkins University
Observed institutions:
Howard Hughes Medical Institute,
Johns Hopkins University,
Johns Hopkins Medicine,
Montreal Children's Hospital,
Johns Hopkins Hospital
OpenAlex ID:
A5111408425
Rhodopsin mutations in autosomal dominant retinitis pigmentosa.
1991
·
C H Sung
, C M Davenport
, et al.
·
Proceedings of the National Academy of Sciences
·
464
Value of combined phenotypic markers in identifying inheritance of familial adenomatous polyposis.
1991
·
F M Giardiello
, G J Offerhaus
, et al.
·
Gut
·
46
PDF
Characterization and Validation of Refillable Episcleral Drug Delivery Devices for Unidirectional and Controlled Transscleral Drug Delivery
2005
·
M. Krause
, R.L. e Silva
, et al.
·
Investigative Ophthalmology & Visual Science
·
2
Multiallelic Inheritance And/or Modifier Alleles in Leber Congenital Amaurosis: Analysis With the Lca Disease Chip
2004
·
Rando Allikmets
, Jana Zernant
, et al.
·
Investigative Ophthalmology & Visual Science
·
2
Sealable Episcleral Drug Delivery Devices. The Effects of Sustained Release Formulations, Laser and Cryo on Ocular Pharmacokinetics of Tracers.
2006
·
Ricardo A P De Carvalho
, Mattea Durst
, et al.
·
Investigative Ophthalmology & Visual Science
·
1
Transscleral Diffusion Patterns and Intraocular Tracer Kinetics of Sealable and Refillable Episcleral Drug Delivery Systems
2005
·
Ricardo A P De Carvalho
, Melissa Krause
, et al.
·
Investigative Ophthalmology & Visual Science
·
1
Candidate Gene Analysis in X–linked Congenital Nystagmus (NYS1)
2004
·
John Kerrison
, Donald J. Zack
, et al.
·
Investigative Ophthalmology & Visual Science
·
1
Monogenic inheritance of Leber congenital amaurosis: causation by a novel mutation in CRB1.
2004
·
Hana Abouzeid
, Y. Li
, et al.
·
Investigative Ophthalmology & Visual Science
·
1
Leber Congenital Amaurosis (LCA) Patients With Possible Mutations in Two Ciliary Genes: CEP290 and RPGRIP1. Does Oligogenic Inheritance Exist in LCA?
2008
·
Robert K. Koenekoop
, Gerald A. Fishman
, et al.
·
Investigative Ophthalmology & Visual Science
Genetic Basis of Extreme Hyperopia
2006
·
Olof Sundin
, Imran Ahmed Bhutto
, et al.
·
Investigative Ophthalmology & Visual Science
Posterior Polar Cataract Caused by a Recurrent Mutation in PITX3
2003
·
Simone Finzi
, Y. Li
, et al.
·
Investigative Ophthalmology & Visual Science
Genotyping Microarray (Disease Chip) for Leber Congenital Amaurosis
2003
·
Rando Allikmets
, Jana Zernant
, et al.
·
Investigative Ophthalmology & Visual Science
Analysis of Developmental Genes in LCA Patients with CRX Mutations and Genotype-Phenotype Correlation
2002
·
Sharola Dharmaraj
, Stacie L. Bumgarner
, et al.
·
Investigative Ophthalmology & Visual Science
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Works count:
13
Citation count:
518
H-index:
2
I10-index:
2
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