Keywords
Last Name
Institution

Kenton R. Holden

Title
InstitutionMedical University of South Carolina
DepartmentNeurology
AddressP.O. Box MSC 616
428 CSB
96 Jonathan Lucas St.
Phone843-792-7031
Fax843-792-9279
vCardDownload vCard

    Collapse Bibliographic 
    Collapse selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    List All   |   Timeline
    1. Hirose T, Cabrera-Socorro A, Chitayat D, Lemonnier T, Féraud O, Cifuentes-Diaz C, Gervasi N, Mombereau C, Ghosh T, Stoica L, Bacha JDA, Yamada H, Lauterbach MA, Guillon M, Kaneko K, Norris JW, Siriwardena K, Blasér S, Teillon J, Mendoza-Londono R, Russeau M, Hadoux J, Ito S, Corvol P, Matheus MG, Holden KR, Takei K, Emiliani V, Bennaceur-Griscelli A, Schwartz CE, Nguyen G, Groszer M. ATP6AP2 variant impairs CNS development and neuronal survival to cause fulminant neurodegeneration. J Clin Invest. 2019 04 15; 129(5):2145-2162. PMID: 30985297.
      View in: PubMed
    2. Larrew T, Eskandari R, Holden KR, Chen A, Spellicy CJ, Jones JR, Lee JA, Lyons MJ. Transgenerational Inheritance of Familial Lipomyelomeningocele. J Child Neurol. 2017 Dec; 32(14):1118-1122. PMID: 29129155.
      View in: PubMed
    3. Brooks M, Holden KR, Durón RM, McElligott JT, Summer A. Feasibility of developing a pediatric telehealth network in Honduras with international consultation support. Rural Remote Health. 2017 Apr-Jun; 17(2):3965. PMID: 28564548.
      View in: PubMed
    4. Samra JA, Hagood NL, Summer A, Medina MT, Holden KR. Clinical Features and Neurologic Complications of Children Hospitalized With Chikungunya Virus in Honduras. J Child Neurol. 2017 07; 32(8):712-716. PMID: 28459170.
      View in: PubMed
    5. Smith JA, Holden KR, Friez MJ, Jones JR, Lyons MJ. A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features. Am J Med Genet A. 2016 12; 170(12):3313-3318. PMID: 27570168.
      View in: PubMed
    6. Molinero I, Broman-Fulks J, Lyons MJ, Matheus MG, Chaubey A, DuPont BR, Friez MJ, Skinner SA, Holden KR. Importance of genetic testing in global health during the evaluation of familial microcephaly. Clin Case Rep. 2016 10; 4(10):968-971. PMID: 27761248.
      View in: PubMed
    7. Roberts DR, Holden KR. Progressive increase of T1 signal intensity in the dentate nucleus and globus pallidus on unenhanced T1-weighted MR images in the pediatric brain exposed to multiple doses of gadolinium contrast. Brain Dev. 2016 Mar; 38(3):331-6. PMID: 26345358.
      View in: PubMed
    8. Catalino MP, Durón RM, Bailey JN, Holden KR. The influence of traditional and complementary and alternative medicine on medication adherence in Honduras. Altern Ther Health Med. 2015 May-Jun; 21(3):26-35. PMID: 26026142.
      View in: PubMed
    9. Matheus MG, Lehman RK, Bonilha L, Holden KR. Redefining the Pediatric Phenotype of X-Linked Monocarboxylate Transporter 8 (MCT8) Deficiency: Implications for Diagnosis and Therapies. J Child Neurol. 2015 Oct; 30(12):1664-8. PMID: 25900139.
      View in: PubMed
    10. Dwivedi AC, Lyons MJ, Kwiatkowski K, Bartel FO, Friez MJ, Holden KR, Fung ET, DuPont BR. Clinical utility of chromosomal microarray analysis in the diagnosis and management of monosomy 7 mosaicism. Mol Cytogenet. 2014; 7(1):93. PMID: 25530805.
      View in: PubMed
    11. Smith AW, Holden KR, Dwivedi A, Dupont BR, Lyons MJ. Deletion of 16q24.1 supports a role for the ATP2C2 gene in specific language impairment. J Child Neurol. 2015 Mar; 30(4):517-21. PMID: 25296922.
      View in: PubMed
    12. Mooneyham KA, Holden KR, Cathey S, Dwivedi A, Dupont BR, Lyons MJ. Neurodevelopmental delays and macrocephaly in 17p13.1 microduplication syndrome. Am J Med Genet A. 2014 Nov; 164A(11):2887-91. PMID: 25123844.
      View in: PubMed
    13. Holden KR. Heads you win, tails you lose: measuring head circumference. Dev Med Child Neurol. 2014 Aug; 56(8):705. PMID: 24660758.
      View in: PubMed
    14. Dean SJ, Holden KR, Dwivedi A, Dupont BR, Lyons MJ. Acquired microcephaly in blepharophimosis-ptosis-epicanthus inversus syndrome because of an interstitial 3q22.3q23 deletion. Pediatr Neurol. 2014 Jun; 50(6):636-9. PMID: 24725350.
      View in: PubMed
    15. Zarate YA, Lichty AW, Champion KJ, Clarkson LK, Holden KR, Matheus MG. Unique cerebrovascular anomalies in Noonan syndrome with RAF1 mutation. J Child Neurol. 2014 Aug; 29(8):NP13-7. PMID: 23877478.
      View in: PubMed
    16. Hayflick SJ, Kruer MC, Gregory A, Haack TB, Kurian MA, Houlden HH, Anderson J, Boddaert N, Sanford L, Harik SI, Dandu VH, Nardocci N, Zorzi G, Dunaway T, Tarnopolsky M, Skinner S, Holden KR, Frucht S, Hanspal E, Schrander-Stumpel C, Mignot C, Héron D, Saunders DE, Kaminska M, Lin JP, Lascelles K, Cuno SM, Meyer E, Garavaglia B, Bhatia K, de Silva R, Crisp S, Lunt P, Carey M, Hardy J, Meitinger T, Prokisch H, Hogarth P. ß-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulation. Brain. 2013 Jun; 136(Pt 6):1708-17. PMID: 23687123.
      View in: PubMed
    17. Davis K, Holden KR, S'Aulis D, Amador C, Matheus MG, Rizzo WB. Novel mutation in Sjogren-Larsson syndrome is associated with divergent neurologic phenotypes. J Child Neurol. 2013 Oct; 28(10):1259-65. PMID: 23034980.
      View in: PubMed
    18. Holden KR, Cooper SL, Wong JG. Neuroscience curriculum changes and outcomes: medical university of South Carolina, 2006 to 2010. Neurologist. 2012 Jul; 18(4):190-5. PMID: 22735242.
      View in: PubMed
    19. Lyons MJ, Fuller JD, Montoya Mdel C, DuPont BR, Holden KR. Unbalanced translocation involving partial trisomy 9p and partial monosomy yq with neurodevelopmental delays. J Child Neurol. 2013 Apr; 28(4):524-6. PMID: 22752474.
      View in: PubMed
    20. Stevenson RE, Holden KR, Rogers RC, Schwartz CE. Seizures and X-linked intellectual disability. Eur J Med Genet. 2012 May; 55(5):307-12. PMID: 22377486.
      View in: PubMed
    21. Lockrow JP, Holden KR, Dwivedi A, Matheus MG, Lyons MJ. LIS1 duplication: expanding the phenotype. J Child Neurol. 2012 Jun; 27(6):791-5. PMID: 22190508.
      View in: PubMed
    22. Burruss DM, Wood TC, Espinoza L, Dwivedi A, Holden KR. Severe Hunter syndrome (mucopolysaccharidosis II) phenotype secondary to large deletion in the X chromosome encompassing IDS, FMR1, and AFF2 (FMR2). J Child Neurol. 2012 Jun; 27(6):786-90. PMID: 22190500.
      View in: PubMed
    23. Dukes-Rimsky L, Guzauskas GF, Holden KR, Griggs R, Ladd S, Montoya Mdel C, DuPont BR, Srivastava AK. Microdeletion at 4q21.3 is associated with intellectual disability, dysmorphic facies, hypotonia, and short stature. Am J Med Genet A. 2011 Sep; 155A(9):2146-53. PMID: 21834054.
      View in: PubMed
    24. Edens AC, Lyons MJ, Duron RM, Dupont BR, Holden KR. Autism in two females with duplications involving Xp11.22-p11.23. Dev Med Child Neurol. 2011 May; 53(5):463-6. PMID: 21418194.
      View in: PubMed
    25. Medina MT, Aguilar-Estrada RL, Alvarez A, Durón RM, Martínez L, Dubón S, Estrada AL, Zúniga C, Cartagena D, Thompson A, Ramirez E, Banegas L, Osorio JR, Delgado-Escueta AV, Collins JS, Holden KR. Reduction in rate of epilepsy from neurocysticercosis by community interventions: the Salamá, Honduras study. Epilepsia. 2011 Jun; 52(6):1177-85. PMID: 21275975.
      View in: PubMed
    26. Schroer RJ, Holden KR, Tarpey PS, Matheus MG, Griesemer DA, Friez MJ, Fan JZ, Simensen RJ, Strømme P, Stevenson RE, Stratton MR, Schwartz CE. Natural history of Christianson syndrome. Am J Med Genet A. 2010 Nov; 152A(11):2775-83. PMID: 20949524.
      View in: PubMed
    27. Skinner HJ, Dubon-Murcia SA, Thompson AR, Medina MT, Edwards JC, Nicholas JS, Holden KR. Adult convulsive status epilepticus in the developing country of Honduras. Seizure. 2010 Jul; 19(6):363-7. PMID: 20554456.
      View in: PubMed
    28. Lyons MJ, Duron R, Molinero I, Sangiuolo F, Holden KR. Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita. Pediatr Neurol. 2010 May; 42(5):365-8. PMID: 20399394.
      View in: PubMed
    29. Rollins JD, Collins JS, Holden KR. United States head circumference growth reference charts: birth to 21 years. J Pediatr. 2010 Jun; 156(6):907-913.e2. PMID: 20304425.
      View in: PubMed
    30. Geer JS, Skinner SA, Goldin E, Holden KR. Mucolipidosis type IV: a subtle pediatric neurodegenerative disorder. Pediatr Neurol. 2010 Mar; 42(3):223-6. PMID: 20159435.
      View in: PubMed
    31. Pollard LM, Williams NR, Espinoza L, Wood TC, Spector EB, Schroer RJ, Holden KR. Diagnosis, treatment, and long-term outcomes of late-onset (type III) multiple acyl-CoA dehydrogenase deficiency. J Child Neurol. 2010 Aug; 25(8):954-60. PMID: 20023066.
      View in: PubMed
    32. Slaughter JL, Espinoza L, Molinero I, Wood TC, Duron C, Flores A, Porter R, Tomashitis K, Holden KR. Utilization of blood spot testing for metabolic-genetic disorders in Honduras: is it time for newborn screening? J Child Neurol. 2010 Mar; 25(3):306-11. PMID: 19850562.
      View in: PubMed
    33. Travaglini L, Brancati F, Attie-Bitach T, Audollent S, Bertini E, Kaplan J, Perrault I, Iannicelli M, Mancuso B, Rigoli L, Rozet JM, Swistun D, Tolentino J, Dallapiccola B, Gleeson JG, Valente EM, Zankl A, Leventer R, Grattan-Smith P, Janecke A, D'Hooghe M, Sznajer Y, Van Coster R, Demerleir L, Dias K, Moco C, Moreira A, Kim CA, Maegawa G, Petkovic D, Abdel-Salam GM, Abdel-Aleem A, Zaki MS, Marti I, Quijano-Roy S, Sigaudy S, de Lonlay P, Romano S, Touraine R, Koenig M, Lagier-Tourenne C, Messer J, Collignon P, Wolf N, Philippi H, Kitsiou Tzeli S, Halldorsson S, Johannsdottir J, Ludvigsson P, Phadke SR, Udani V, Stuart B, Magee A, Lev D, Michelson M, Ben-Zeev B, Fischetto R, Benedicenti F, Stanzial F, Borgatti R, Accorsi P, Battaglia S, Fazzi E, Giordano L, Pinelli L, Boccone L, Bigoni S, Ferlini A, Donati MA, Caridi G, Divizia MT, Faravelli F, Ghiggeri G, Pessagno A, Briguglio M, Briuglia S, Salpietro CD, Tortorella G, Adami A, Castorina P, Lalatta F, Marra G, Riva D, Scelsa B, Spaccini L, Uziel G, Del Giudice E, Laverda AM, Ludwig K, Permunian A, Suppiej A, Signorini S, Uggetti C, Battini R, Di Giacomo M, Cilio MR, Di Sabato ML, Leuzzi V, Parisi P, Pollazzon M, Silengo M, De Vescovi R, Greco D, Romano C, Cazzagon M, Simonati A, Al-Tawari AA, Bastaki L, Mégarbané A, Sabolic Avramovska V, de Jong MM, Stromme P, Koul R, Rajab A, Azam M, Barbot C, Martorell Sampol L, Rodriguez B, Pascual-Castroviejo I, Teber S, Anlar B, Comu S, Karaca E, Kayserili H, Yüksel A, Akcakus M, Al Gazali L, Sztriha L, Nicholl D, Woods CG, Bennett C, Hurst J, Sheridan E, Barnicoat A, Hennekam R, Lees M, Blair E, Bernes S, Sanchez H, Clark AE, DeMarco E, Donahue C, Sherr E, Hahn J, Sanger TD, Gallager TE, Dobyns WB, Daugherty C, Krishnamoorthy KS, Sarco D, Walsh CA, McKanna T, Milisa J, Chung WK, De Vivo DC, Raynes H, Schubert R, Seward A, Brooks DG, Goldstein A, Caldwell J, Finsecke E, Maria BL, Holden K, Cruse RP, Swoboda KJ, Viskochil D. Expanding CEP290 mutational spectrum in ciliopathies. Am J Med Genet A. 2009 Oct; 149A(10):2173-80. PMID: 19764032.
      View in: PubMed
    34. Molinero MR, Holden KR, Rodriguez LC, Collins JS, Samra JA, Shinnar S. Pediatric convulsive status epilepticus in Honduras, Central America. Epilepsia. 2009 Oct; 50(10):2314-9. PMID: 19694798.
      View in: PubMed
    35. Hudspeth MP, Joseph S, Holden KR. A novel mutation in type II methemoglobinemia. J Child Neurol. 2010 Jan; 25(1):91-3. PMID: 19471045.
      View in: PubMed
    36. Durón RM, Medina MT, Nicolás O, Varela FE, Ramírez F, Battle SJ, Thompson A, Rodríguez LC, Oseguera C, Aguilar-Estrada RL, Pietsch-Escueta S, Collins JS, Holden KR. Adherence and complementary and alternative medicine use among Honduran people with epilepsy. Epilepsy Behav. 2009 Apr; 14(4):645-50. PMID: 19435580.
      View in: PubMed
    37. Gregory ML, Guzauskas GF, Edgar TS, Clarkson KB, Srivastava AK, Holden KR. A novel GLRA1 mutation associated with an atypical hyperekplexia phenotype. J Child Neurol. 2008 Dec; 23(12):1433-8. PMID: 19073849.
      View in: PubMed
    38. Mohebbi MR, Holden KR, Butler IJ. FIRST: a practical approach to the causes and management of febrile seizures. J Child Neurol. 2008 Dec; 23(12):1484-8. PMID: 19073858.
      View in: PubMed
    39. Kossoff EH, Dorward JL, Molinero MR, Holden KR. The modified Atkins diet: a potential treatment for developing countries. Epilepsia. 2008 Sep; 49(9):1646-7. PMID: 18782218.
      View in: PubMed
    40. Amador C, Mathews AM, Del Carmen Montoya M, Laughridge ME, Everman DB, Holden KR. Expanding the neurologic phenotype of oculodentodigital dysplasia in a 4-generation Hispanic family. J Child Neurol. 2008 Aug; 23(8):901-5. PMID: 18660473.
      View in: PubMed
    41. Cantagrel V, Silhavy JL, Bielas SL, Swistun D, Marsh SE, Bertrand JY, Audollent S, Attié-Bitach T, Holden KR, Dobyns WB, Traver D, Al-Gazali L, Ali BR, Lindner TH, Caspary T, Otto EA, Hildebrandt F, Glass IA, Logan CV, Johnson CA, Bennett C, Brancati F, Valente EM, Woods CG, Gleeson JG. Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. Am J Hum Genet. 2008 Aug; 83(2):170-9. PMID: 18674751.
      View in: PubMed
    42. Rogers RC, Stevenson RE, Simensen RJ, Holden KR, Schwartz CE. Finding new etiologies of mental retardation and hypotonia: X marks the spot. Dev Med Child Neurol. 2008 Feb; 50(2):104-11. PMID: 18190539.
      View in: PubMed
    43. Giurgiutiu DV, Espinoza LM, Wood TC, DuPont BR, Holden KR. Persistent growth failure in Prader-Willi syndrome associated with short-chain acyl-CoA dehydrogenase gene variant. J Child Neurol. 2008 Jan; 23(1):112-7. PMID: 18184946.
      View in: PubMed
    44. Smith AW, Glenn RC, Williams V, Kostova F, Holden KR, Gillespie CF, Boutwell B, Richard GV, Maria BL. What do future (female) pediatricians value? J Pediatr. 2007 Nov; 151(5):443-4, 444.e1-2. PMID: 17961680.
      View in: PubMed
    45. Lyons MJ, Wood T, Espinoza L, Stensland HM, Holden KR. Early onset alpha-mannosidosis with slow progression in three Hispanic males. Dev Med Child Neurol. 2007 Nov; 49(11):854-7. PMID: 17979865.
      View in: PubMed
    46. Lance EI, DuPont BR, Holden KR. Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007 Sep; 22(9):1124-7. PMID: 17890413.
      View in: PubMed
    47. Medina MT, Munsat T, Portera-Sánchez A, Durón RM, Becker CA, Holden KR. Developing a neurology training program in Honduras: a joint project of neurologists in Honduras and the World Federation of Neurology. J Neurol Sci. 2007 Feb 15; 253(1-2):7-17. PMID: 17188302.
      View in: PubMed
    48. Addison PK, Berry V, Holden KR, Espinal D, Rivera B, Su H, Srivastava AK, Bhattacharya SS. A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic family. Mol Vis. 2006 Jul 20; 12:791-5. PMID: 16885921.
      View in: PubMed
    49. Hudspeth MP, Holden KR, Crawford TO. The "slurp" test: bedside evaluation of bulbar muscle fatigue. Pediatrics. 2006 Aug; 118(2):e530-3. PMID: 16847079.
      View in: PubMed
    50. Dodds JA, Srivastava AK, Holden KR. Unusual phenotypic expression of an XLRS1 mutation in X-linked juvenile retinoschisis. J Child Neurol. 2006 Apr; 21(4):331-3. PMID: 16900931.
      View in: PubMed
    51. Yallapragada AV, Cure JK, Holden KR. Sturge-Weber syndrome variant with atypical intracranial findings: case report. J Child Neurol. 2006 Feb; 21(2):155-7. PMID: 16566882.
      View in: PubMed
    52. Vajsar J, Zhang W, Dobyns WB, Biggar D, Holden KR, Hawkins C, Ray P, Olney AH, Burson CM, Srivastava AK, Schachter H. Carriers and patients with muscle-eye-brain disease can be rapidly diagnosed by enzymatic analysis of fibroblasts and lymphoblasts. Neuromuscul Disord. 2006 Feb; 16(2):132-6. PMID: 16427280.
      View in: PubMed
    53. Holden KR, Zuñiga OF, May MM, Su H, Molinero MR, Rogers RC, Schwartz CE. X-linked MCT8 gene mutations: characterization of the pediatric neurologic phenotype. J Child Neurol. 2005 Oct; 20(10):852-7. PMID: 16417886.
      View in: PubMed
    54. Bhat SS, Rogers RC, Holden KR, Srivastava AK. A novel in-frame deletion in ARX is associated with lissencephaly with absent corpus callosum and hypoplastic genitalia. Am J Med Genet A. 2005 Sep 15; 138(1):70-2. PMID: 16097002.
      View in: PubMed
    55. Mohebbi MR, Holden KR. Interleukin-1beta and febrile seizures: from bench to bedside. Ann Neurol. 2005 Apr; 57(4):608-9. PMID: 15786470.
      View in: PubMed
    56. Mohebbi MR, Holden KR. Febrile and afebrile or provoked and unprovoked seizures? Pediatr Neurol. 2005 Apr; 32(4):291; author reply 291-2. PMID: 15797192.
      View in: PubMed
    57. Medina MT, Durón RM, Martínez L, Osorio JR, Estrada AL, Zúniga C, Cartagena D, Collins JS, Holden KR. Prevalence, incidence, and etiology of epilepsies in rural Honduras: the Salamá Study. Epilepsia. 2005 Jan; 46(1):124-31. PMID: 15660778.
      View in: PubMed
    58. Vervoort VS, Holden KR, Ukadike KC, Collins JS, Saul RA, Srivastava AK. POMGnT1 gene alterations in a family with neurological abnormalities. Ann Neurol. 2004 Jul; 56(1):143-8. PMID: 15236414.
      View in: PubMed
    59. Mohammadi M, Mohebbi MR, Holden KR. Facial hemangioma, and associated malformations: a case report. Neuropediatrics. 2004 Jun; 35(3):194-7. PMID: 15248103.
      View in: PubMed
    60. Mohebbi MR, Holden KR, Mohammadi M. Peripheral leukocytosis in children with febrile seizures. J Child Neurol. 2004 Jan; 19(1):47-50. PMID: 15032384.
      View in: PubMed
    61. Cason AL, Ikeguchi Y, Skinner C, Wood TC, Holden KR, Lubs HA, Martinez F, Simensen RJ, Stevenson RE, Pegg AE, Schwartz CE. X-linked spermine synthase gene (SMS) defect: the first polyamine deficiency syndrome. Eur J Hum Genet. 2003 Dec; 11(12):937-44. PMID: 14508504.
      View in: PubMed
    62. Molinero MR, Varon D, Holden KR, Sladky JT, Molina IB, Cleaves F. Epidemiology of childhood Guillain-Barré syndrome as a cause of acute flaccid paralysis in Honduras: 1989-1999. J Child Neurol. 2003 Nov; 18(11):741-7. PMID: 14696900.
      View in: PubMed
    63. Holden KR, Collins JS, Greene JF, Hinkle S, Nave AF, Portillo JM, Page GP, Stevenson RE. Dietary intake and blood folate levels in Honduran women of childbearing age. J Child Neurol. 2002 May; 17(5):341-6. PMID: 12150580.
      View in: PubMed
    64. Dobson SR, Holden KR, Nietert PJ, Cure JK, Laver JH, Disco D, Abboud MR. Moyamoya syndrome in childhood sickle cell disease: a predictive factor for recurrent cerebrovascular events. Blood. 2002 May 01; 99(9):3144-50. PMID: 11964276.
      View in: PubMed
    65. Hahn KA, Salomons GS, Tackels-Horne D, Wood TC, Taylor HA, Schroer RJ, Lubs HA, Jakobs C, Olson RL, Holden KR, Stevenson RE, Schwartz CE. X-linked mental retardation with seizures and carrier manifestations is caused by a mutation in the creatine-transporter gene (SLC6A8) located in Xq28. Am J Hum Genet. 2002 May; 70(5):1349-56. PMID: 11898126.
      View in: PubMed
    66. Holden KR, Titus MO, Van Tassel P. Cranial magnetic resonance imaging examination of normal term neonates: a pilot study. J Child Neurol. 1999 Nov; 14(11):708-10. PMID: 10593546.
      View in: PubMed
    67. Dobyns WB, Berry-Kravis E, Havernick NJ, Holden KR, Viskochil D. X-linked lissencephaly with absent corpus callosum and ambiguous genitalia. Am J Med Genet. 1999 Oct 08; 86(4):331-7. PMID: 10494089.
      View in: PubMed
    68. Holden KR, Titus MO. The effect of tiagabine on spasticity in children with intractable epilepsy: a pilot study. Pediatr Neurol. 1999 Oct; 21(4):728-30. PMID: 10580885.
      View in: PubMed
    69. Wagner CL, Eicher DJ, Katikaneni LD, Barbosa E, Holden KR. The use of hypothermia: a role in the treatment of neonatal asphyxia? Pediatr Neurol. 1999 Jul; 21(1):429-43. PMID: 10428427.
      View in: PubMed
    70. Adams AB, Tyor WR, Holden KR. Interferon beta-1b and childhood multiple sclerosis. Pediatr Neurol. 1999 Jul; 21(1):481-3. PMID: 10428435.
      View in: PubMed
    71. Anderson DL, Spratt EG, Macias MM, Jellinek MS, Murphy JM, Pagano M, Griesemer DA, Holden KR, Barbosa E. Use of the pediatric symptom checklist in the pediatric neurology population. Pediatr Neurol. 1999 Feb; 20(2):116-20. PMID: 10082339.
      View in: PubMed
    72. Moreland EC, Griesemer DA, Holden KR. Topiramate for intractable childhood epilepsy. Seizure. 1999 Feb; 8(1):38-40. PMID: 10091847.
      View in: PubMed
    73. Holden KR, Sessions JC, Curé J, Whitcomb DS, Sade RM. Neurologic outcomes in children with post-pump choreoathetosis. J Pediatr. 1998 Jan; 132(1):162-4. PMID: 9470021.
      View in: PubMed
    74. Van Tassel P, Curé JK, Holden KR. Cystlike white matter lesions in tuberous sclerosis. AJNR Am J Neuroradiol. 1997 Aug; 18(7):1367-73. PMID: 9282871.
      View in: PubMed
    75. Holden KR, Clarke SL, Griesemer DA. Long-term outcomes of conventional therapy for infantile spasms. Seizure. 1997 Jun; 6(3):201-5. PMID: 9203248.
      View in: PubMed
    76. Willi SM, Zhang Y, Hill JB, Phelan MC, Michaelis RC, Holden KR. A deletion in the long arm of chromosome 18 in a child with serum carnosinase deficiency. Pediatr Res. 1997 Feb; 41(2):210-3. PMID: 9029640.
      View in: PubMed
    77. Psenka TM, Holden KR. Benign familial neonatal convulsions; psychosocial adjustment to the threat of recurrent seizures. Seizure. 1996 Sep; 5(3):243-5. PMID: 8902929.
      View in: PubMed
    78. Gurecki PJ, Holden KR, Sahn EE, Dyer DS, Cure JK. Developmental neural abnormalities and seizures in epidermal nevus syndrome. Dev Med Child Neurol. 1996 Aug; 38(8):716-23. PMID: 8761167.
      View in: PubMed
    79. Abboud MR, Jackson SM, Barredo J, Holden KR, Cure J, Laver J. Neurologic complications following bone marrow transplantation for sickle cell disease. Bone Marrow Transplant. 1996 Mar; 17(3):405-7. PMID: 8704695.
      View in: PubMed
    80. Joseph M, Pai GS, Holden KR, Herman G. X-linked myotubular myopathy: clinical observations in ten additional cases. Am J Med Genet. 1995 Nov 06; 59(2):168-73. PMID: 8588581.
      View in: PubMed
    81. Lucas JW, Holden KR, Purohit DM, Cure JK. Neonatal hemangiomatosis associated with brachial plexus palsy. J Child Neurol. 1995 Sep; 10(5):411-3. PMID: 7499765.
      View in: PubMed
    82. Curé JK, Holden KR, Van Tassel P. Progressive venous occlusion in a neonate with Sturge-Weber syndrome: demonstration with MR venography. AJNR Am J Neuroradiol. 1995 Aug; 16(7):1539-42. PMID: 7484651.
      View in: PubMed
    83. Washington EC, Ector W, Abboud M, Ohning B, Holden K. Hemolytic jaundice due to G6PD deficiency causing kernicterus in a female newborn. South Med J. 1995 Jul; 88(7):776-9. PMID: 7597488.
      View in: PubMed
    84. Basco WT, Abboud M, Holden KR. Opsoclonus-myoclonus and recurrent neuroblastoma. J Pediatr. 1995 May; 126(5 Pt 1):847-8. PMID: 7752022.
      View in: PubMed
    85. Parsons JL, Sahn EE, Holden KR, Pai GS. Neurologic disease in a child with hepatoerythropoietic porphyria. Pediatr Dermatol. 1994 Sep; 11(3):216-21. PMID: 7971555.
      View in: PubMed
    86. Holden KR, Jabs EW, Sponseller PD. Roberts/pseudothalidomide syndrome and normal intelligence: approaches to diagnosis and management. Dev Med Child Neurol. 1992 Jun; 34(6):534-9. PMID: 1612213.
      View in: PubMed
    87. Holden KR. Childhood epilepsy: an overview. J S C Med Assoc. 1992 May; 88(5):251-5. PMID: 1602752.
      View in: PubMed
    88. Shinnar S, Vining EP, Mellits ED, D'Souza BJ, Holden K, Baumgardner RA, Freeman JM. Discontinuing antiepileptic medication in children with epilepsy after two years without seizures. A prospective study. N Engl J Med. 1985 Oct 17; 313(16):976-80. PMID: 4047105.
      View in: PubMed
    89. Mellits ED, Holden KR, Freeman JM. Neonatal seizures. II. A multivariate analysis of factors associated with outcome. Pediatrics. 1982 Aug; 70(2):177-85. PMID: 7099783.
      View in: PubMed
    90. Holden KR, Mellits ED, Freeman JM. Neonatal seizures. I. Correlation of prenatal and perinatal events with outcomes. Pediatrics. 1982 Aug; 70(2):165-76. PMID: 7099782.
      View in: PubMed
    91. Emerson R, D'Souza BJ, Vining EP, Holden KR, Mellits ED, Freeman JM. Stopping medication in children with epilepsy: predictors of outcome. N Engl J Med. 1981 May 07; 304(19):1125-9. PMID: 7219445.
      View in: PubMed
    92. Holden KR, Freeman JM. Neonatal seizures and their treatment. Clin Perinatol. 1975 Mar; 2(1):3-13. PMID: 1102217.
      View in: PubMed
    93. Zimmerman AW, Holden KR, Reiter EO, Dekaban AS. Medroxprogesterone acetate in the treatment of seizures associated with menstruation. J Pediatr. 1973 Dec; 83(6):959-63. PMID: 4757534.
      View in: PubMed
    94. Dekaban AS, Holden KR, Constantopoulos G. Effects of fresh plasma or whole blood transfusions on patients with various types of mucopolysaccharidosis. Pediatrics. 1972 Nov; 50(5):688-92. PMID: 4263750.
      View in: PubMed
    95. Holden KR, Dekaban AS. Neurological involvement in nevus unis lateris and nevus linearis sebaceus. Neurology. 1972 Sep; 22(9):879-87. PMID: 4117264.
      View in: PubMed
    96. Holden KR, Young RB, Piland JH, Hurt WG. Plasma pressors in the normal and stressed newborn infant. Pediatrics. 1972 Apr; 49(4):495-503. PMID: 5062521.
      View in: PubMed
    97. Holden KR, Alexander F. Diffuse neonatal hemangiomatosis. Pediatrics. 1970 Sep; 46(3):411-21. PMID: 5465931.
      View in: PubMed
    Holden's Networks
    Click the "See All" links for more information and interactive visualizations!
    Concepts Expand Description
    _
    Co-Authors Expand Description
    _
    Similar People Expand Description
    _
    Same Department Expand Description
    Physical Neighbors Expand Description
    _