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1

Diagnostic Distinctions and Genetic Analysis of Patients Diagnosed with Moebius Syndrome

MacKinnon, Sarah, Oystreck, Darren T., Andrews, Caroline, Chan, Wai-Man, Hunter, David G., Engle, Elizabeth C.

Journal:

Year:

2014

Language:

english

File:

PDF, 1.68 MB

english, 2014

2

Diagnostic ophthalmologic findings in Moebius syndrome

Mackinnon, Sarah E., Oystreck, Darren T., Andrews, Caroline V., Engle, Elizabeth C., Hunter, David G.

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2013

Language:

english

File:

PDF, 67 KB

english, 2013

3

Partial Duplication of Chromosome 19 Associated with Syndromic Duane Retraction Syndrome

Abu-Amero, Khaled K., Kondkar, Altaf A., Al Otaibi, Abdullah, Alorainy, Ibrahim A., Khan, Arif O., Hellani, Ali M., Oystreck, Darren T., Bosley, Thomas M.

Journal:

Ophthalmic Genetics

Year:

2015

Language:

english

File:

PDF, 689 KB

english, 2015

4

The clinical spectrum of homozygous HOXA1 mutations

Thomas M. Bosley, Ibrahim A. Alorainy, Mustafa A. Salih, Hesham M. Aldhalaan, Khaled K. Abu-Amero, Darren T. Oystreck, Max A. Tischfield, Elizabeth C. Engle, Robert P. Erickson

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 134 KB

english, 2008

5

Molecular and neurological characterizations of three Saudi families with lipoid proteinosis

Mustafa A Salih, Khaled K Abu-Amero, Saleh Alrasheed, Ibrahim A Alorainy, Lu Liu, John A McGrath, Lionel Van Maldergem, Yasser H Al-Fakey, Adel H AlSuhaibani, Darren T Oystreck, Thomas M Bosley

Journal:

BMC Medical Genetics

Year:

2011

Language:

english

File:

PDF, 625 KB

english, 2011

6

Homozygous HOXA1 mutations disrupt human brainstem, inner ear, cardiovascular and cognitive development

Tischfield, Max A, Bosley, Thomas M, Salih, Mustafa A M, Alorainy, Ibrahim A, Sener, Emin C, Nester, Michael J, Oystreck, Darren T, Chan, Wai-Man, Andrews, Caroline, Erickson, Robert P

Journal:

Nature Genetics

Year:

2005

Language:

english

File:

PDF, 234 KB

english, 2005

7

Diplopia following cataract surgery: a review of 150 patients

Nayak, H, Kersey, J P, Oystreck, D T, Cline, R A, Lyons, C J

Journal:

Year:

2007

Language:

english

File:

PDF, 134 KB

english, 2007

8

HOXB1 Founder Mutation in Humans Recapitulates the Phenotype of Hoxb1−/− Mice

Bryn D. Webb, Sherin Shaaban, Harald Gaspar, Luis F. Cunha, Christian R. Schubert, Ke Hao, Caroline D. Robson, Wai-Man Chan, Caroline Andrews, Sarah MacKinnon, Darren T. Oystreck, David G. Hunter, Ant

Journal:

The American Journal of Human Genetics

Year:

2012

Language:

english

File:

PDF, 726 KB

english, 2012

9

Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3

T.M. Bosley, M.A. Salih, J.C. Jen, D.D. Lin, D. Oystreck, K.K. Abu-Amero, D.B. MacDonald, Z. al Zayed, H. al Dhalaan, T. Kansu, B. Stigsby, R.W. Baloh

Journal:

American Journal of Ophthalmology

Year:

2005

Language:

english

File:

PDF, 37 KB

english, 2005

10

Fixation Preference for the Affected Eye in Patients With Unilateral Duane Syndrome

Arif O. Khan, Darren T. Oystreck

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2006

Language:

english

File:

PDF, 66 KB

english, 2006

11

Clinical Characteristics of Bilateral Duane Syndrome

Arif O. Khan, Darren Oystreck

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2006

Language:

english

File:

PDF, 90 KB

english, 2006

12

Ophthalmologic features of ataxia telangiectasia-like disorder due to homozygous MRE11 mutation

Arif O. Khan, Darren T. Oystreck, Mustafa Salih

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2007

Language:

english

File:

PDF, 45 KB

english, 2007

13

Ophthalmic features of ataxia telangiectasia–like disorder

Arif O. Khan, Darren T. Oystreck, Michel Koenig, Mustafa A. Salih

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2008

Language:

english

File:

PDF, 605 KB

english, 2008

14

Long-term Results of an Intraoperative Adjustable Superior Oblique Tendon Suture Spacer Using Nonabsorbable Suture for Brown Syndrome

Donny W. Suh, Darren T. Oystreck, David G. Hunter

Journal:

Year:

2008

Language:

english

File:

PDF, 136 KB

english, 2008

15

Ophthalmic Features of Joubert Syndrome

Arif O. Khan, Darren T. Oystreck, Mohamed Z. Seidahmed, Abdulmajeed AlDrees, Salah A. Elmalik, Ibrahim A. Alorainy, Mustafa A. Salih

Journal:

Year:

2008

Language:

english

File:

PDF, 298 KB

english, 2008

16

Bilateral Synergistic Convergence Associated with Homozygous ROB03 Mutation (p.Pro771Leu)

Arif O. Khan, Darren T. Oystreck, Nada Al-Tassan, Latifa Al-Sharif, Thomas M. Bosley

Journal:

Year:

2008

Language:

english

File:

PDF, 939 KB

english, 2008

17

Acute acquired comitant esotropia: A prospective study

Lyons, Christopher J, Tiffin, Peter A C, Oystreck, Darren

Journal:

Year:

1999

Language:

english

File:

PDF, 419 KB

english, 1999

18

Notices of Books.

Oystreck, Darren T., Morales, Jose, Chaudhry, Imtiaz, Alorainy, Ibrahim A., Elkhamary, Sahar M., Pasha, Taha M.U., Bosley, Thomas M.

Journal:

Year:

1891

Language:

english

File:

PDF, 398 KB

english, 1891

19

Visual Loss in Orbitofacial Neurofibromatosis Type 1

Oystreck, Darren T., Morales, Jose, Chaudhry, Imtiaz, Alorainy, Ibrahim A., Elkhamary, Sahar M., Pasha, Taha M.U., Bosley, Thomas M.

Journal:

Year:

2012

Language:

english

File:

PDF, 1.05 MB

english, 2012

20

Comitant strabismus: Perspectives, present and future

Oystreck, Darren T., Lyons, Christopher J.

Journal:

Saudi Journal of Ophthalmology

Year:

2012

Language:

english

File:

PDF, 644 KB

english, 2012

21

When straight eyes won't move: phenotypic overlap of genetically distinct ocular motility disturbances

Oystreck, Darren T., Salih, Mustafa A., Bosley, Thomas M.

Journal:

Canadian Journal of Ophthalmology / Journal Canadien d'Ophtalmologie

Year:

2011

File:

PDF, 501 KB

2011

22

Presbyopia complicating pre-existing strabismus

Oystreck, Darren T., Lyons, Christopher J.

Journal:

Canadian Journal of Ophthalmology / Journal Canadien d'Ophtalmologie

Year:

2003

Language:

english

File:

PDF, 632 KB

english, 2003

23

Ocular motility abnormalities in orbitofacial neurofibromatosis type 1

Oystreck, Darren T., Alorainy, Ibrahim A., Morales, Jose, Chaudhry, Imtiaz A., Elkhamary, Sahar M., Bosley, Thomas M.

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2014

Language:

english

File:

PDF, 805 KB

english, 2014

24

Duane Retraction Syndrome on the Arabian Peninsula

Khan, Arif O., Oystreck, Darren T., Wilken, Keith, Akbar, Fatima

Journal:

Year:

2007

Language:

english

File:

PDF, 1.35 MB

english, 2007

25

Partial chromosome 7 duplication with a phenotype mimicking the HOXA1 spectrum disorder

Abu-Amero, Khaled K., Kondkar, Altaf A., Salih, Mustafa A. M., Alorainy, Ibrahim A., Khan, Arif O., Oystreck, Darren T., Bosley, Thomas M.

Journal:

Ophthalmic Genetics

Year:

2013

Language:

english

File:

PDF, 739 KB

english, 2013

26

Ophthalmologic Observations in a Patient with Partial Mosaic Trisomy 8

Abu-Amero, Khaled K., Kondkar, Altaf A., Salih, Mustafa A., Al-Husain, Muneera, Al Shammari, Muneera, Zeidan, Ghassan, Oystreck, Darren T., Hellani, Ali M., Kentab, Amal Y., Bosley, Thomas M.

Journal:

Ophthalmic Genetics

Year:

2013

Language:

english

File:

PDF, 866 KB

english, 2013

27

A newly recognized autosomal recessive syndrome affecting neurologic function and vision

Salih, Mustafa A., Tzschach, Andreas, Oystreck, Darren T., Hassan, Hamdy H., AlDrees, Abdulmajeed, Elmalik, Salah A., El Khashab, Heba Y., Wienker, Thomas F., Abu-Amero, Khaled K., Bosley, Thomas M.

Journal:

American Journal of Medical Genetics Part A

Year:

2013

Language:

english

File:

PDF, 774 KB

english, 2013

28

CCDD Phenotype Associated with a Small Chromosome 2 Deletion

Abu-Amero, Khaled K., Bosley, Thomas M., Kondkar, Altaf A., Oystreck, Darren T., Khan, Arif O.

Journal:

Seminars in Ophthalmology

Year:

2014

Language:

english

File:

PDF, 439 KB

english, 2014

29

Recent Progress in Understanding Congenital Cranial Dysinnervation Disorders

Oystreck, Darren T, Engle, Elizabeth C, Bosley, Thomas M

Journal:

Journal of Neuro-Ophthalmology

Year:

2011

Language:

english

File:

PDF, 718 KB

english, 2011

30

Congenital cranial dysinnervation disorders

Bosley, Thomas M., Abu-Amero, Khaled K., Oystreck, Darren T.

Journal:

Current Opinion in Ophthalmology

Year:

2013

Language:

english

File:

PDF, 253 KB

english, 2013

31

Congenital Myasthenic Syndrome Due to Homozygous CHRNE Mutations: Report of Patients in Arabia

Salih, Mustafa A, Oystreck, Darren T, Al-Faky, Yasser H, Kabiraj, Mohammed, Omer, Mohamed I A, Subahi, Elamin M, Beeson, David, Abu-Amero, Khaled K, Bosley, Thomas M

Journal:

Journal of Neuro-Ophthalmology

Year:

2011

Language:

english

File:

PDF, 328 KB

english, 2011

32

Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3

Bosley, T. M., Salih, M. A.M., Jen, J. C., Lin, D. D.M., Oystreck, D., Abu-Amero, K. K., MacDonald, D. B., al Zayed, Z., al Dhalaan, H., Kansu, T., Stigsby, B., Baloh, R. W.

Journal:

Year:

2005

Language:

english

File:

PDF, 613 KB

english, 2005

33

Variable Ptosis after Botulinum Toxin Type A Injection with Positive Ice Test Mimicking Ocular Myasthenia Gravis

Alaraj, Ahmad M., Oystreck, Darren T., Bosley, Thomas M.

Journal:

Journal of Neuro-Ophthalmology

Year:

2013

Language:

english

File:

PDF, 163 KB

english, 2013

34

Xq26.3 Microdeletion in a Male with Wildervanck Syndrome

Abu-Amero, Khaled K., Kondkar, Altaf A., Alorainy, Ibrahim A., Khan, Arif O., Al-Enazy, Leila A., Oystreck, Darren T., Bosley, Thomas M.

Journal:

Ophthalmic Genetics

Year:

2014

Language:

english

File:

PDF, 797 KB

english, 2014

35

Microdeletions involving Chromosomes 12 and 22 Associated with Syndromic Duane Retraction Syndrome

Abu-Amero, Khaled K., Kondkar, Altaf A., Oystreck, Darren T., Khan, Arif O., Bosley, Thomas M.

Journal:

Ophthalmic Genetics

Year:

2014

Language:

english

File:

PDF, 705 KB

english, 2014

36

Clinical characterization of the HOXA1 syndrome BSAS variant

Bosley, T. M., Salih, M. A., Alorainy, I. A., Oystreck, D. T., Nester, M., Abu-Amero, K. K., Tischfield, M. A., Engle, E. C.

Journal:

Year:

2007

Language:

english

File:

PDF, 501 KB

english, 2007

37

Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome

Abu-Amero, Khaled K., Kondkar, Altaf, Hellani, Ali M., Oystreck, Darren T., Khan, Arif O., Bosley, Thomas M.

Journal:

Ophthalmic Genetics

Year:

2015

Language:

english

File:

PDF, 499 KB

english, 2015

38

Orbitofacial neurofibromatosis: clinical characteristics and treatment outcome

Chaudhry, I A, Morales, J, Shamsi, F A, Al-Rashed, W, Elzaridi, E, Arat, Y O, Jacquemin, C, Oystreck, D T, Bosley, T M

Journal:

Year:

2012

Language:

english

File:

PDF, 544 KB

english, 2012

39

Retinal Dysfunction in Patients with Congenital Fibrosis of the Extraocular Muscles Type 2

Khan, Arif O., Almutlaq, Mohammed, Oystreck, Darren T., Engle, Elizabeth C., Abu-Amero, Khaled, Bosley, Thomas

Journal:

Ophthalmic Genetics

Year:

2015

Language:

english

File:

PDF, 748 KB

english, 2015

40

The neurology of carbonic anhydrase type II deficiency syndrome

Bosley, T. M., Salih, M. A., Alorainy, I. A., Islam, M. Z., Oystreck, D. T., Suliman, O. S. M., Malki, S. a., Suhaibani, A. H., Khiari, H., Beckers, S., van Wesenbeeck, L., Perdu, B., AlDrees, A., Elm

Journal:

Year:

2011

Language:

english

File:

PDF, 837 KB

english, 2011

41

A novel syndrome caused by the E410K amino acid substitution in the neuronal -tubulin isotype 3

Chew, S., Balasubramanian, R., Chan, W.-M., Kang, P. B., Andrews, C., Webb, B. D., MacKinnon, S. E., Oystreck, D. T., Rankin, J., Crawford, T. O., Geraghty, M., Pomeroy, S. L., Crowley, W. F., Jabs, E

Journal:

Year:

2013

Language:

english

File:

PDF, 762 KB

english, 2013

42

Duane retraction syndrome in a patient with Duchenne muscular dystrophy

Bosley, Thomas M., Salih, Mustafa A., Alkhalidi, Hisham, Oystreck, Darren T., El Khashab, Heba Y., Kondkar, Altaf A., Abu-Amero, Khaled K.

Journal:

Ophthalmic Genetics

Year:

2016

Language:

english

File:

PDF, 757 KB

english, 2016

43

Duane Retraction Syndrome Associated with a Small X Chromosome Deletion

Abu-Amero, Khaled K., Kondkar, Altaf A., Odan, Hessa al, Khan, Arif O., Oystreck, Darren T., Bosley, Thomas M.

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2016

Language:

english

File:

PDF, 131 KB

english, 2016

44

HOXA1 Mutations are Not Commonly Associated with Non-Syndromic Deafness

Abu-Amero, Khaled K., Hagr, Abdulrahman al, Almomani, Murad O., Azad, Taif Anwar, Alorainy, Ibrahim A., Oystreck, Darren T., Bosley, Thomas M.

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2014

File:

PDF, 160 KB

2014

45

Neurologic Injury in Isolated Sulfite Oxidase Deficiency

Bosley, Thomas M., Alorainy, Ibrahim A., Oystreck, Darren T., Hellani, Ali M., Seidahmed, Mohammed Z., Osman, Mohamed El Faki, Sabry, Mohamed A., Rashed, Mohamed S., Al-Yamani, Eiman A., Abu-Amero, Kh

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2014

File:

PDF, 8.08 MB

2014

46

The genetics of nonsyndromic bilateral Duane retraction syndrome

Abu-Amero, Khaled K., Khan, Arif O., Oystreck, Darren T., Kondkar, Altaf A., Bosley, Thomas M.

Journal:

Journal of American Association for Pediatric Ophthalmology and Strabismus

Year:

2016

Language:

english

File:

PDF, 214 KB

english, 2016

47

Correspondence

Lyons, Christopher, Tiffin, Peter, Oystreck, Darren

Journal:

Year:

2000

Language:

english

File:

PDF, 87 KB

english, 2000

48

Ophthalmoplegia and Congenital Cranial Dysinnervation Disorders

Oystreck, Darren T.

Journal:

Journal of Binocular Vision and Ocular Motility

Year:

2018

Language:

english

File:

PDF, 606 KB

english, 2018

49

Congenital and Genetic Ocular Motility Disorders: Update and Considerations

Oystreck, Darren

Journal:

American Orthoptic Journal

Year:

2015

Language:

english

File:

PDF, 1.03 MB

english, 2015

50

Synergistic Divergence: A Distinct Ocular Motility Dysinnervation Pattern

Oystreck, Darren T., Khan, Arif O., Vila-Coro, Antonio Aguirre, Oworu, Olugbemisola, Al-Tassan, Nada, Chan, Wai-Man, Engle, Elizabeth C., Bosley, Thomas M.

Journal:

Investigative Ophthalmology & Visual Science

Year:

2009

Language:

english

File:

PDF, 496 KB

english, 2009

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