D. Pillers

发表

A novel dystrophin isoform is required for normal retinal electrophysiology.

P. Ray, T. M. Nguyen, W. Karges, 1995, Human molecular genetics.

Familial IgA nephropathy.

R. Koler, D. Pillers, 1985, The New England journal of medicine.

Gram-negative pathogen Klebsiella oxytoca is associated with spontaneous chronic otitis media in Toll-like receptor 4-deficient C3H/HeJ mice

D. Trune, J. Pang, C. MacArthur, 2008, Acta oto-laryngologica.

DXS28 (C7) maps centromeric to DXS68 (L1-4) and DXS67 (B24) by deletion analysis.

J. Towbin, E. McCabe, W. Seltzer, 1990, Genomics.

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

C. Westall, P. Ray, B. Powell, 1994, Ophthalmology.

Cochlear Cytokine Gene Expression in Murine Acute Otitis Media

J. B. Kempton, D. Trune, D. Pillers, 2007, The Laryngoscope.

Hearing loss in the laminin-deficient dy mouse model of congenital muscular dystrophy.

J. B. Kempton, D. Trune, J. Pang, 2002, Molecular genetics and metabolism.

Dystrophin and the retina.

D. Pillers, 1999, Molecular genetics and metabolism.

MINIREVIEW Dystrophin and the Retina

D. Pillers, 1999 .

Cerebral blood oxygenation measurement in sheep brain In-vivo using transfontanelle photoacoustic spectroscopy

F. Charbel, Rayyan Manwar, Kamran Avanaki, 2022, BiOS.

Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations

P. Ray, B. Powell, R. Schnur, 1999, Human Genetics.

mdx Cv3 Mouse Is a Model for Electroretinography of Duchenne/Becker Muscular Dystrophy

D. G. Green, V. Chapman, W. Woodward, 1995 .

Negative-configuration electroretinogram in Oregon eye disease. Consistent phenotype in Xp21 deletion syndrome.

F. Tremblay, E. McCabe, P. Ray, 1993, Archives of ophthalmology.

Interstitial duplication of the short arm of chromosome 1 in a newborn with congenital heart disease and multiple malformations.

J. Gilhooly, M. Rice, C. Warden, 2001, American journal of medical genetics.

A°land Island Eye Disease (Forsius-Eriksson Syndrome) Associated With Contiguous Deletion Syndrome at Xp21: Similarity to Incomplete Congenital Stationary Night Blindness

B. Powell, R. Magenis, R. Weleber, 1989 .

Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophy.

J. Towbin, E. McCabe, B. Powell, 1990, American journal of human genetics.

Potential for Misdiagnosis Due to Lack of Metabolic Derangement in Combined Methylmalonic Aciduria/Hyperhomocysteinemia (cblC) in the Neonate

R. Steiner, K. Gibson, T. Bottiglieri, 2003, Journal of Perinatology.

Velo-cardio-facial syndrome and DiGeorge sequence with meningomyelocele and deletions of the 22q11 region.

R. Nickel, B. Emanuel, D. Driscoll, 1994, American journal of medical genetics.

PCR methods in clinical investigations of human ureaplasmas: a minireview.

T. Colaizy, D. Pillers, T. Kuforiji, 2003, Molecular genetics and metabolism.

OA1 mutations and deletions in X-linked ocular albinism.

K. Kidd, G. Quinn, S. Orlow, 1998, American journal of human genetics.

Aland Island eye disease (Forsius-Eriksson ocular albinism) and an Xp21 deletion in a patient with Duchenne muscular dystrophy, glycerol kinase deficiency, and congenital adrenal hypoplasia.

B. Powell, R. Magenis, R. Weleber, 1990, American journal of medical genetics.

Isoflurane is an effective alternative to ketamine/xylazine/acepromazine as an anesthetic agent for the mouse electroretinogram

W. Woodward, Dongseok Choi, Sawan Hurst, 2007, Documenta Ophthalmologica.

Normal photoresponses and altered b-wave responses to APB in the mdxCv3 mouse isolated retina ERG supports role for dystrophin in synaptic transmission

D. G. Green, D. Pillers, Hao Guo, 2004, Visual Neuroscience.

Dystrophin expression in the human retina is required for normal function as defined by electroretinography

C. Westall, D. Bulman, P. Ray, 1993, Nature Genetics.

Interstitial deletions of the short arm of chromosome 4 in patients with a similar combination of multiple minor anomalies and mental retardation.

J. Reiss, R. Magenis, M. Brown, 1995, American journal of medical genetics.

Subgaleal hematoma: the need for increased awareness of risk.

G. Benda, N. Binder, J. Gilhooly, 1995, The Journal of family practice.

Meiotic exchange event within the stalk region of an inverted chromosome 22 results in a recombinant chromosome with duplication of the distal long arm

J. Gilhooly, R. Magenis, H. Lawce, 2005, American journal of medical genetics. Part A.

Effects of dystrophin isoforms on signal transduction through neural retina: genotype-phenotype analysis of duchenne muscular dystrophy mouse mutants.

D. G. Green, V. Chapman, D. Hood, 1999, Molecular genetics and metabolism.

Localization of dystrophin isoform Dp71 to the inner limiting membrane of the retina suggests a unique functional contribution of Dp71 in the retina.

P. Ray, R. Weleber, P. Howard, 1998, Human molecular genetics.

Redefinition of dystrophin isoform distribution in mouse tissue by RT-PCR implies role in nonmuscle manifestations of duchenne muscular dystrophy.

A. Sadeghi, A. Sadeghi, S. Tokarz, 1998, Molecular genetics and metabolism.

Cochlear Cytokine Gene Expression in Murine Chronic Otitis Media

J. Beth Kempton, Dennis R. Trune, D. Trune, 2007, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Altered expression of middle and inner ear cytokines in mouse otitis media

D. Trune, J. Pang, C. MacArthur, 2011, The Laryngoscope.

Normal Cochlear Function in mdx and mdxCv3 Duchenne Muscular Dystrophy Mouse Models

D. Trune, D. Pillers, S. Dwinnell, 1999, The Laryngoscope.

mdxCv3 mouse is a model for electroretinography of Duchenne/Becker muscular dystrophy.

D. G. Green, V. Chapman, W. Woodward, 1995, Investigative ophthalmology & visual science.

Detection of Ureaplasma DNA in Endotracheal Samples Is Associated With Bronchopulmonary Dysplasia After Adjustment for Multiple Risk Factors

J. Lapidus, T. Colaizy, Cynthia D. Morris, 2007, Pediatric Research.

Achieved Versus Intended Pulse Oximeter Saturation in Infants Born Less Than 28 Weeks' Gestation: The AVIOx Study

Christopher H Schmid, C. Schmid, D. Phelps, 2006, Pediatrics.

Maternal and Newborn Hospital Outcomes of Perinatal SARS-CoV-2 Infection: A National Registry.

Eileen M. Walsh, Melissa A. Babilonia-Rosa, Kathryn M. Kauffman, 2023, Pediatrics.

Hb Hope [beta 136(H14) Gly----Asp] and Hb E [beta 26(B8)Glu----Lys]: compound heterozygosity in a Thai Mien family.

R. Jones, C. Head, D. Pillers, 1992, Hemoglobin.

Misleading hepatitis C serology following administration of intravenous immunoglobulin.

Rebecca Lynn Johnson, R. Nixon, D. Pillers, 1994, American journal of clinical pathology.

Lung ultrasound may allow for timelier surfactant administration and reduce radiograph use.

D. Pillers, 2019, The Journal of pediatrics.

Development of ex vivo brain hemorrhage phantom for photoacoustic imaging

Rayyan Manwar, M. T. Islam, A. Shoo, 2023, Journal of Biophotonics.

28 Weeks' Gestation: The AVIOx Study Achieved Versus Intended Pulse Oximeter Saturation in Infants Born Less Than

C. Schmid, D. Phelps, J. Hagadorn, 2013 .

Aland Island eye disease (Forsius-Eriksson syndrome) associated with contiguous deletion syndrome at Xp21. Similarity to incomplete congenital stationary night blindness.

B. Powell, R. Magenis, R. Weleber, 1989, Archives of ophthalmology.