Stead Family Department of Pediatrics

Arlene V. Drack, MD

Portrait

Ronald V. Keech, MD, Associate Professor in Ophthalmic Genetics
Director, Pediatric Electroretinogram Service
Associate Professor of Ophthalmology and Visual Sciences
Associate Professor of Pediatrics

Contact Information

Office: 11190-G PFP
Iowa City, IA 52242

Lab: 4111  MERF
Iowa City, IA 52242
Phone: 319-353-5507

Email: arlene-drack@uiowa.edu

Education

BS, Biology / Philosophy, University of Scranton
MD, Medicine, The Pennsylvania State University College of Medicine

Fellowship, ITT International Fellow, Immunology, Det Norske Radiumhospitalet, University of Oslo
Internship, Transitional Internship, Georgetown University Medical Center
Fellowship, Ophthalmic Genetics, Wilmer Institute, Johns Hopkins University
Residency, Ophthalmology, Georgetown University Medical Center
Fellowship, Pediatric Ophthalmology and Strabismus, University of Iowa, Department of Ophthalmology
Fellowship, Molecular Ophthalmic Genetics, University of Iowa

Licensure and Certifications

Medical License, Iowa Board of Medicine
Medical License (inactive), Colorado Board of Medical Examiners
Medical License (inactive), Georgia Composite Medical Board
ABO Certification, American Board of Ophthalmology
NBME Diplomate, National Board of Medical Examiners

Education/Training Program Affiliations

Biosciences Graduate Program
Interdisciplinary Graduate Program in Genetics
Interdisciplinary Graduate Program in Neuroscience

Research Summary

Arlene V. Drack, M.D. is a clinician scientist specializing in juvenile inherited eye diseases. She is the inaugural Ronald V. Keech Associate Professor in Pediatric Ophthalmic Genetics at the University of Iowa Department of Ophthalmology and Visual Sciences. Her research focuses on inherited eye diseases that affect children, particularly in the development of novel treatments. She is experienced in subretinal injection of molecules to treat mouse models of retinal degeneration, as well as participating in human trials for retinal disorders. She co-directs both the clinical and rodent electroretinogram services at the University of Iowa. Her clinical practice includes the full scope of pediatric ophthalmology and strabismus, in addition to running specialized genetic eye disease clinics.

Center, Program and Institute Affiliations

John and Marcia Carver Nonprofit Genetic Testing Laboratory
Stephen A. Wynn Institute for Vision Research

All Publications

Zhang Y, Seo S, Bhattarai S, Bugge K, Searby C, Zhange Q, Drack A, Stone E, Sheffield V.  BBS mutations modify phenotypic expression of CEP290-related ciliopathies.  Hum Mol Genet.  2014. 23(1):40-51.
[Link]

Shubert C, Pryds A, Zeng S, Xie Y, Bailey , Freund K, Spaide R, Merriam J, Barbazetto I, Slakter J, Chang S, Munch I, Drack A, Hernandez J, Yzer S, Merriam J, Linneberg A, Larsen M, Yannuzzi L, Mullins R, Allikmets R.  Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy.  Hum Mutat.  2014. 35(7):859-67.
[PubMed]

Schubert C, Pryds A, Zeng S, Xie Y, Freund K, Spaide R, Merriam J, Barbazetto I, Slakter J, Chang S, Munch I, Drack A, Hernandez J, Yzer S, Merriam J, Linneberg A, Larsen M, Yannuzzi L, Mullins R, Allikmets R.  Cadherin 5 is Regulated by Corticosteroids and Associated with Central Serous Chorioretinopathy.  Hum Mutat.  2014. 35(7):859-867.
[PubMed]

Burnight E, Wiley L, Drack A, Braun T, Anfinson K, Kaalberg E, Halder J, Affatigato L, Mullins R, Stone E, Tucker B.  CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype..  Gene Ther.  2014. 21(7):662-72.
[PubMed]

Drack A, Rabinowitz Y, Cotlier E.  Congenital cataracts and genetic anomalies of the lens, Chapter 137.  Academic Press.  2014. 

Drack A, Mullins R, Pfeifer W, Augustine E, Stasheff S, Hong S.  Immunosuppressive Treatment for Retinal Degeneration in Juvenile Neuronal Ceroid Lipofuscinosis (Juvenile Batten Disease).  Ophthalmic Genet.  2014. 
[PubMed]

Mullins R, Khanna A, Shoo D, Tucker B, Sohn E, Drack A, Stone E.  Is age-related macular degeneration a microvascular disease?.  Adv Exp Med Biol.  2014. 801:283-289.
[PubMed]

Mullins R, Khanna A, Schoo D, Tucker B, Sohn E, Drack A, Stone E.  Is age-related macular degeneration a microvascular disease?.  Adv Exp Med Biol.  2014. 801:283-9.
[PubMed]

Ramachandran P, Ghattarai S, Singh P, Boudreau R, Thompson S, Laspada A, Drack A, Davidson B.  RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degeneration. .  PloS one;  2014. 

Kemp P, Larson S, Drack A.  Strabismus surgery in patients receiving warfarin anticoagulation.  J AAPOS.  2014. 18(1):84-6.
[PubMed]

Pan Y, Bhattarai S, Modestou M, Drack A, Chetkovich D, Baker S.  TRIP8b Is Required for Maximal Expression of HCN1 in the Mouse Retina.  PloS one.  2014. 9(1):e85850.
[Link]

Stunkel M, Bhattarai S, Kemerley A, Stone E, Wang K, Mullins R, Drack A.  Vitritis in Pediatric Genetic Retinal Disorders .  Ophthalmology.  2014. 
[PubMed]

McAnany J, Genead M, Walia S, Drack A, Stone E, Koenekoop R, Traboulsi E, Smith A, Weleber R, Jacobson S, Fishman G.  Visual Acuity Changes in Patients With Leber Congenital Amaurosis and Mutations in CEP290..  JAMA Ophthalmol. .  2013 February 1. 131(2):178-82.
[PubMed]

Drack A, Miller J, Pearce D.  A Novel c.1135_1138delCTGT Mutation in CLN3 Leads to Juvenile Neuronal Ceroid Lipofuscinosis.  J Child Neurol.  2013. 28(9):1112-1116.
[Link]

Stone E, Aldave A, Drack A, MacCumber M, Sheffield V, Traboulsi E, Weleber R.  Author reply: To PMID 22944025.  Ophthalmology.  2013. 120(10):e73.
[PubMed]

Drack A, Mullins R, Seo S.  Bardet Biedl Syndrome.  Lippincott Williams & Wilkins.  2013. 

Drack A, Rabinowitz Y, Cotlier E.  Congenital cataracts and genetic anomalies of the lens. (Chapter 137).  Academic Press.  2013. 

Stasheff S, Blodi F, Shankar M, Bennicelli J, Bennett J, Bhatarrai S, Thompson S, Drack A.  Early Rpe65 Gene Therapy More Effectively Restores Precise Visual Responses to Retinal Ganglion Cells of Rpe65-/- mice in vitro [Abstract].  Ann Neurol.  2013. 74:S129.

Chamling X, Seo S, Bugge K, Searby C, Guo D, Drack A, Rahmouni K, Sheffield V.  Ectopic Expression of Human BBS4 Can Rescue Bardet-Biedl Syndrome Phenotypes in Bbs4 Null Mice.  PLoS One.  2013. 8(3):e59101.
[PubMed]

Seo S, Bhattarai S, Gratie D, Stone E, Sheffield V, Mullins R, Drack A.  Gene therapy in a mouse model of Bardet Biedl Syndrome type I.  IOVS.  2013. 

Tucker B, Mullins R, Streb L, Anfinson K, Eyestone M, Kaalberg E, Riker M, Drack A, Braun T, Stone E.  Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa.  eLife.  2013. 2:e00824.
[Link]

Drack A, Mullins R, Seo S.  Retinitis Pigmentosa Syndromes: Bardet-Biedl Syndrome.  Lippincott Williams & Williams.  2013. 

Seo S, Mullins R, Dumitrescu A, Bhattarai S, Gratie D, Wang K, Stone E, Sheffield V, Drack A.  Subretinal gene therapy of mice with Bardet-Biedl Syndrome type 1.  Invest Ophthalmol Vis Sci.  2013. 54(9):6118-6132.
[Link]

Drack A.  Traumatic iritis.  American Academy of Pediatrics.  2013. 

Stone E, Aldave A, Drack A, Maccumber M, Sheffield V, Traboulsi E, Weleber R.  Recommendations for genetic testing of inherited eye diseases: report of the American Academy of Ophthalmology task force on genetic testing.  Ophthalmology.  2012 November. 119(11):2408-10.
[PubMed]

Dumitrescu A, Milunsky J, Longmuir S, Drack A.  A family with branchio-oculo-facial syndrome with primarily ocular involvement associated with mutation of the TFAP2A gene.  Ophthalmic Genet.  2012 June. 33(2):100-6.
[PubMed]

Drack A, Dumitrescu A, Bhattarai S, Gratie D, Stone E, Mullins R, Sheffield V.  TUDCA slows retinal degeneration in two different mouse models of retinitis pigmentosa and prevents obesity in Bardet-Biedl type 1 mice.  Invest Ophthalmol Vis Sci.  2012 May. 53(1):396-402.
[PubMed]

Dumitrescu A, Moga D, Olson R, Longmuir S, Drack A.  Author Reply.  Ophthalmology.  2012. 119(5):1089-90.
[PubMed]

Zhang M, Hutchinson A, Drack A, Cleveland J, Lambert S.  Improved Ocular Alignment with Adjustable Sutures in Adults Undergoing Strabismus Surgery.  Ophthalmology.  2012. 119(2):396-402.
[PubMed]

Drack A.  Trauma leading to pain, photophobia, and small pupil.  American Academy of Pediatrics.  2012. 

Dumitrescu A, Moga D, Longmuir S, Olson R, Drack A.  Prevalence and characteristics of abnormal head posture in children with Down syndrome: a 20-year retrospective, descriptive review.  Ophthalmology.  2011 September. 118(9):1859-64.
[Link]

Capo H, Repka M, Edmond J, Drack A, Blumenfield L, Sjatkowski R.  Optic nerve abnormalities in children: a practical approach.  J AAPOS.  2011 June. 15(3):281-90.
[PubMed]

Lachke S, Alkuraya F, Kneeland S, Ohn T, Aboukhalil A, Howell G, Saadi I, Cavallesco R, Yue Y, Tsai A, Nair K, Cosma M, Smith R, Hodges E, Alfadhli S, Al-Hajeri A, Shamseldin H, Behbehani A, Hannon G, Bulyk M, Drack A, Anderson P, John S, Maas R.  Mutations in the RNA granule component TDRD7 cause cataract and glaucoma.  Science.  2011 March 25. 331(6024):1571-6.
[Link]

Milunsky J, Maher T, Zhao G, Wang Z, Mulliken J, Chitayat D, Clemens M, Stalker H, Bauer M, Burch M, Chénier S, Cunningham M, Drack A, Janssens S, Karlea A, Klatt R, Kini U, Klein O, Lachmeijer A, Megarbane A, Mendelsohn N, Meschino W, Mortier G, Parkash S, Ray C, Roberts A, Roberts A, Reardon W, Schnur R, Smith R, Splitt M, Tezcan K, Whiteford M, Wong D, Zori R, Lin A.  Genotype-phenotype analysis of the branchio-oculo-facial syndrome.  Am J Med Genet A.  2011 January. 155A(1):22-32.
[Link]

Narkewicz M, Rosenthal P, Schwarz K, Drack A, Margolis T, Repka M, PEDS-C Study Group .  Ophthalmologic complications in children with chronic hepatitis C treated with pegylated interferon.  J Pediatr Gastroenterol Nutr.  2010 August. 51(2):183-6.
[Link]

Drack A, Lambert S, Stone E.  From the Laboratory to the Clinic: Molecular Genetic Testing in Pediatric Ophthalmology.  Am J Ophthal.  2010. 149(1):10-17.
[PubMed]

Zein W, Drack A.  Inheritance of Refractive Errors.  Oxford University Press.  2010. 

Narkewicz M, Rosenthal P, Schwarz K, Drack A, Margolis T, Repka M.  PEDS-C Study Group.  J Pediatr Gastroenterol Nutr.  2010. 51(2):183-186.

Walia S, Fishman G, Jacobson S, Aleman T, Koenekoop R, Traboulsi E, Weleber R, Pennesi M, Heon E, Drack A, Lam B, Allikmets R, Stone E.  Visual Acuity in Patients with Leber Congenital Amaurosis and Early Childhood-Onset Retinitis Pigmentosa.  Ophthalmol.  2010. 117(6):1190-8.
[PubMed]

Drack A, Johnston R, Stone E.  Which Leber congenital amaurosis patients are eligible for gene therapy trials?.  J AAPOS.  2009 October. 13(5):463-5.
[Link]

Hink E, Oliver S, Drack A, Hawes M, Wojno T, On A, Durairaj V.  Pediatric golf-related ophthalmic injuries.  Arch Ophthalmol.  2008 September. 126(9):1252-6.
[Link]

Drack A.  Refractive Errors in Children.  Elsevier.  2008. 

Drack A.  Refractive Errors in Children.  2007. 

Curtis T, Stout A, Drack A, Durairaj V.  Giant orbital cysts after strabismus surgery.  Am J Ophthalmol.  2006 October. 142(4):697-9.
[Link]

Prall F, Drack A, Taylor M, Ku L, Olson J, Gregory D, Mestroni L, Mandava N.  Ophthalmic manifestations of Danon disease.  Ophthalmology.  2006 June. 113(6):1010-3.
[Link]

Sands R, Drack A.  Pediatric Ophthalmology, Chapter 15: Eye.  2006. 

Drack A.  Retinopathy of prematurity.  Adv Pediatr.  2006. 53:211-26.
[Link]

Drack A.  Pediatric Ophthalmology, Chapter 13.  Mosby.  2005. 

Lambert S, Drack A, Hutchinson A.  Longitudinal changes in the refractive errors of children with tears in Descemet's membrane following forceps injuries.  J AAPOS.  2004 August. 8(4):368-70.
[Link]

Dubois L, Drack A.  Ocular Genetics.  Refinements (JCAHPO modules).  2004. 4(1):1-12.

Sands R, Drack A, Eisenbaum A.  Pediatric Ophthalmology.  2004. 

Dracl A.  Heritable disorders of RPE, Bruch's membrane, and the choriocapillaris.  Springer.  2002. 

Drack A.  Myopia.  Springer.  2002. 

Reddy C, Drack A.  Nonvascular Hamartomas.  Springer.  2002. 

Drack A.  Patterns of Retinal Disease in Children.  Springer.  2002. 

Drack A, Kimura A.  Retinitis Pigmentosa and Associated Disorders.  Springer.  2002. 

Ober R, Palmer E, Wright K, Drack A.  Retinopathy of Prematurity.  Springer.  2002. 

Kerrison J, Giorda R, Lenart T, Drack A, Maumenee I.  Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1).  Ophthalmic Genet.  2001 December. 22(4):241-8.
[Link]

Nucci P, Drack A.  Refractive surgery for unilateral high myopia in children.  J AAPOS.  2001 December. 5(6):348-51.
[Link]

Lambert S, Lynn M, Drews-Botsch C, Loupe D, Plager D, Medow N, Wilson M, Buckley E, Drack A, Fawcett S.  A comparison of grating visual acuity, strabismus, and reoperation outcomes among children with aphakia and pseudophakia after unilateral cataract surgery during the first six months of life.  J AAPOS.  2001 April. 5(2):70-5.
[Link]

Aaberg Jr T, Fallaha N, Drack A, Lambert S.  Clincial outcome of confluent laser photoablation for retinopathy of prematurity [Abstract].  Invest Ophthalmol Vis Sci.  2001. 42(Suppl):S681.

Drack A, Nucci P.  Refractive surgery in children.  Ophthalmology Clinics of North America.  2001. 14(3):457-466.
[PubMed]

Bech-Hansen N, Naylor M, Maybaum T, Sparkes R, Koop B, Birch D, Bergen A, Prinsen C, Polomeno R, Gal A, Drack A, Musarella M, Jacobson S, Young R, Weleber R.  Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.  Nat Genet.  2000 November. 26(3):319-23.
[Link]

Mendicino M, Lynch M, Drack A, Beck A, Harbin T, Pollard Z, Vela M, Lynn M.  Long-term surgical and visual outcomes in primary congenital glaucoma: 360 degrees trabeculotomy versus goniotomy.  J AAPOS.  2000 August. 4(4):205-10.
[Link]

Whitfill C, Drack A.  Avoidance and treatment of retinopathy of prematurity.  Semin Pediatr Surg.  2000 May. 9(2):103-5.
[Link]

Lambert S, Capone A, Cingle K, Drack A.  Cataract and phthisis bulbi after laser photoablation for threshold retinopathy of prematurity.  Am J Ophthalmol.  2000 May. 129(5):585-91.
[Link]

Lenart T, Drack A, Tarnuzzer R, Fernandes A, Lambert S.  Heterochromia after pediatric cataract surgery.  J AAPOS.  2000 February. 4(1):40-5.
[Link]

Drack A, Alcorn D, Lingua R.  Potential Use of LASIK in children.  J Pediatr Ophthalmol Strabismus.  2000. 37(6):354-360.
[PubMed]

Moore C, Drack A.  Prism adaptation in decompensated monofixation syndrome.  Am Orthop J.  2000. 50:80-84.

Srivistava S, Sheridan J, Drack A, Stone E, Saperstein D.  RDS mutation (TRP316STOP) results in butterfly pattern macular dystrophy om am African-American family [Abstract].  Invest Ophthalmol Vis Sci.  2000. 41(Suppl):4709.

Mendicino M, Lynch M, Drack A, Beck A, Harbin T, Pollard Z, Vela M, Lynn M.  Visual outcomes in primary congenital glaucoma: 360 degrees trabeculotomy versus goniotomy.  J AAPOS.  2000. 4:205-210.

Hutcheson K, Drack A, Ellish N, Lambert S.  Anterior hyaloid face opacification after pediatric Nd:YAG laser capsulotomy.  J AAPOS.  1999 October. 3(5):303-7.
[Link]

Drack A, Petronio J, Capone A.  Unilateral retinal hemorrhages in documented cases of child abuse.  Am J Ophthalmol.  1999 September. 128(3):340-4.
[Link]

Chang J, Spraul C, Lynn M, Drack A, Grossniklaus H.  The two-stage mutation model in retinal hemangioblastoma.  Ophthalmic Genet.  1998 September. 19(3):123-30.
[Link]

Drack A, Awosika A, Edelhauser H.  Endothelial cell counts in pediatric eyes with anterior segment abnormalities [Abstract].  Invest Ophthalmol Vis Sci.  1998. 39(Suppl):S54.

Drack A.  Inheritance of Refractive Errors.  Mosby.  1998. 

Drack A.  Preventing blindness in premature infants.  New Engl J Med.  1998. 338(22):1620-1621.
[PubMed]

Hutcheson K, Drack A.  The diagnosis and management of the child who doesn't see.  Focal Points (American Academy of Ophthalmology).  1998. 16(2):1-14.

Hutcheson K, Drack A, Lambert S.  Balloon dilatation for treatment of resistant nasolacrimal duct obstruction.  J AAPOS.  1997 December. 1(4):241-4.
[Link]

Sorkin J, Shoffner J, Grossniklaus H, Drack A, Lambert S.  Strabismus and mitochondrial defects in chronic progressive external ophthalmoplegia.  Am J Ophthalmol.  1997 February. 123(2):235-42.
[Link]

Drack A.  Infantile Cataracts. Indications for systemic and genetic workup.  Am Orthoptic Journal.  1997. 47:2-7.

Drack A.  Pediatric Ophthalmology, Chapter 12.  Mosby.  1997. 

Sorkin J, Davis P, Meacham L, Parks J, Drack A, Lambert S.  Optic nerve hypoplasia: absence of posterior pituitary bright signal on magnetic resonance imaging correlates with diabetes insipidus.  Am J Ophthalmol.  1996 November. 122(5):717-23.
[Link]

Drack A.  Basics of Inheritance.  Lippincott.  1996. 3(Revised Edition):1-17.

Lambert S, Drack A.  Infantile cataracts.  Surv Ophthalmol.  1996. 40(6):427-58.
[Link]

Sorkin J, Davis P, Meacham L, Parks J, Drack A, Lambert S.  Optic nerve hypoplasia: Absence of posterior pituitary bright signal on magnetic resonance imaging correlates with diabetes insipidus.  Correspondence.  1996. 122:717-723.

Drack A.  Congenital and Childhood Macular Lesions.  International Ophthalmology Clinics.  1995. 35(4):1-8.
[PubMed]

Drack A.  Myopia.  Mosby.  1995. 

Drack A, Stone E.  Patterns of Retinal Disease in Children.  Mosby.  1995. 

Kimura A, Drack A, Stone E.  Retinitis Pigmentosa and Associated Disorders.  Mosby.  1995. 

Stone E, Nichols B, Kimura A, Weingeist T, Drack A, Sheffield V.  Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.  Arch Ophthalmol.  1994 June. 112(6):765-72.
[Link]

Drack A, Kutschke P, Stair S, Scott W.  Compliance with safety glasses wear in monocular children.  J Ophthalmic Nurs Technol.  1994. 13(2):77-82.
[Link]

Drack A, Capone Jr A, Fernandes A.  Effects of diode laser photoablation of peripheral retina on the neonatal monkey [Abstract].  Invest Ophthalmol Vis Sci.  1994. 34(suppl):1441.

Reddy V, Capone Jr A, Drack A.  The role of light toxicity in retinopathy of prematurity and congenital cataract.  Am J Ophthalmol.  1994. 117(2):262-264.
[PubMed]

Capone A, Drack A.  Transient lens change after diode laser retinal photoablation for retinopathy of prematurity.  Am J Ophthalmol.  1994. 118(4):533-535.
[PubMed]

Nichols B, Drack A, Vandenburgh K, Kimura A, Sheffield V, Stone E.  A 2 base pair deletion in the RDS Gene Associated with Butterfly-Shaped pigment dystrophy of the fovea.  Hum Mol Genet.  1993. 2(5):601-3.

Nichols B, Sheffield V, Vandenburgh K, Drack A, Kimura A, Stone E.  Butterfly-shaped pigment dystrophy of the fovea is caused by a point mutation in codon 167 of the RDS gene.  Nature Genetics.  1993. 3(2):202-207.
[PubMed]

Johnson A, Drack A, Kwitek A, Cannon R, Stone E, Alward W.  Clinical features and linkage analysis of a family with autosomal dominant juvenile glaucoma.  Ophthalmology.  1993. 100(4):524-529.
[PubMed]

Drack A, Keech R.  Complete cataract.  Mosby.  1993. 

Drack A, Kutschke P, Stair S, Scott W.  Compliance with safety glasses wear in monocular children.  J Pediatr Ophthalmol Strabismus.  1993. 30(4):249-52.
[Link]

Sheffield V, Stone E, Alward W, Drack A, Johnson A, Streb L, Nichols B.  Genetic linkage of familial open angle glaucoma to chromosome 1q21-q31.  Nat Genet.  1993. 4(1):47-50.
[PubMed]

Drack A, Keech R.  Partial cataract.  Mosby.  1993. 

Drack A, Scott W.  A curved, hinged ruler for measurement along the globe.  Arch Ophthalmol.  1992 August. 110(8):1175.
[Link]

Drack A, Traboulsi E, Maumenee I.  Progression of Retinopathy in olivopontocerebellar atrophy with retinal degeneration.  Arch Ophthalmol.  1992. 110(5):712-713.
[PubMed]

Drack A, Burke J, Pulido J, Keech R.  Transient punctuate lenticular opacities as a complication of argon laser photoablation in an infant with retinopathy of prematurity.  Am J Ophthalmol.  1992. 113(5):583-584.
[PubMed]

Drack A, Traboulsi E.  Systemic associations of pigmentary retinopathy.  Int Ophthalmol Clin.  1991. 31(3):35-59.
[PubMed]

Chrousos G, Drack A, Young M, Kattah J, Sirdofsky M.  Neuroretinitis in cat scratch disease.  J Clin Neuroophthalmol.  1990 June. 10(2):92-4.
[Link]

O'Neil J, Drack A.  Rubella: German Measles.  Lippincott Co.  1990. 

O'Neil J, Drack A.  The Eye and Rubella.  Lippincott Co.  1990. 

Weinstein J, Drack A, VerHoeve J, Balaban C.  Saccade amplitude and direction influences on the human presaccadic potential.  Clin Vision Science.  1988. 3(3):203-212.

Vinson J, Possanza C, Drack A.  The effect of ascorbic acid on galactose induced cataracts.  Nutrition Reports Int.  1988. 33:665-66.

Weinstein J, Williams G, Drack A, Stank T, Balaban C.  Cortical evoked potentials preceding voluntary saccadic eye movements.  Neuro-Ophthalmol.  1984. 4(3):169-176.

Ruud E, Beiske K, Drack A, Steen H, Godal T.  Different fate of antibodies to surface IgM and IgD in germinal centre cell-associated lymphomas.  Scand J Immunol .  1984. 19(5):447-455.
[PubMed]

Beiske K, Ruud E, Drack A, Marton P, Godal T.  Induction of maturation of human B-cell lymphomas in vitro: morphologic changes in relation to immunoglobulin and DNA synthesis.  Am J Pathol.  1984. 115(3):362-374.
[PubMed]

Date Last Modified: 06/07/2014 - 21:56:23