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Peter Huttenlocher

AddressChicago IL 60637
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    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.
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    1. Raja Beharelle A, Dick AS, Josse G, Solodkin A, Huttenlocher PR, Levine SC, Small SL. Left hemisphere regions are critical for language in the face of early left focal brain injury. Brain. 2010 Jun; 133(Pt 6):1707-16. PMID: 20466762.
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    2. Levine SC, Kraus R, Alexander E, Suriyakham LW, Huttenlocher PR. IQ decline following early unilateral brain injury: a longitudinal study. Brain Cogn. 2005 Nov; 59(2):114-23. PMID: 16040179.
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    3. O'Connor SE, Kwiatkowski DJ, Roberts PS, Wollmann RL, Huttenlocher PR. A family with seizures and minor features of tuberous sclerosis and a novel TSC2 mutation. Neurology. 2003 Aug 12; 61(3):409-12. PMID: 12913212.
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    4. Huttenlocher PR. Basic neuroscience research has important implications for child development. Nat Neurosci. 2003 Jun; 6(6):541. PMID: 12771955.
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    5. Poussaint TY, Fox JW, Dobyns WB, Radtke R, Scheffer IE, Berkovic SF, Barnes PD, Huttenlocher PR, Walsh CA. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings. Pediatr Radiol. 2000 Nov; 30(11):748-55. PMID: 11100490.
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    6. Huttenlocher PR. The neuropathology of phenylketonuria: human and animal studies. Eur J Pediatr. 2000 Oct; 159 Suppl 2:S102-6. PMID: 11043154.
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    7. Chu D, Huttenlocher PR, Levin DN, Towle VL. Reorganization of the hand somatosensory cortex following perinatal unilateral brain injury. Neuropediatrics. 2000 Apr; 31(2):63-9. PMID: 10832579.
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    8. Gleeson JG, Luo RF, Grant PE, Guerrini R, Huttenlocher PR, Berg MJ, Ricci S, Cusmai R, Wheless JW, Berkovic S, Scheffer I, Dobyns WB, Walsh CA. Genetic and neuroradiological heterogeneity of double cortex syndrome. Ann Neurol. 2000 Feb; 47(2):265-9. PMID: 10665503.
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    9. Fox JW, Lamperti ED, Eksioglu YZ, Hong SE, Feng Y, Graham DA, Scheffer IE, Dobyns WB, Hirsch BA, Radtke RA, Berkovic SF, Huttenlocher PR, Walsh CA. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia. Neuron. 1998 Dec; 21(6):1315-25. PMID: 9883725.
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    10. Precht KS, Lese CM, Spiro RP, Huttenlocher PR, Johnston KM, Baker JC, Christian SL, Kittikamron K, Ledbetter DH. Two 22q telomere deletions serendipitously detected by FISH. J Med Genet. 1998 Nov; 35(11):939-42. PMID: 9832042.
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    11. Huttenlocher PR, Dabholkar AS. Regional differences in synaptogenesis in human cerebral cortex. J Comp Neurol. 1997 Oct 20; 387(2):167-78. PMID: 9336221.
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    12. Staba MJ, Goldman S, Johnson FL, Huttenlocher PR. Allogeneic bone marrow transplantation for Alexander's disease. Bone Marrow Transplant. 1997 Aug; 20(3):247-9. PMID: 9257894.
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    13. Gokhale R, Huttenlocher PR, Brady L, Kirschner BS. Use of barbiturates in the treatment of cyclic vomiting during childhood. J Pediatr Gastroenterol Nutr. 1997 Jul; 25(1):64-7. PMID: 9226529.
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    14. Eksioglu YZ, Scheffer IE, Cardenas P, Knoll J, DiMario F, Ramsby G, Berg M, Kamuro K, Berkovic SF, Duyk GM, Parisi J, Huttenlocher PR, Walsh CA. Periventricular heterotopia: an X-linked dominant epilepsy locus causing aberrant cerebral cortical development. Neuron. 1996 Jan; 16(1):77-87. PMID: 8562093.
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    15. Cao Y, Vikingstad EM, Huttenlocher PR, Towle VL, Levin DN. Functional magnetic resonance studies of the reorganization of the human hand sensorimotor area after unilateral brain injury in the perinatal period. Proc Natl Acad Sci U S A. 1994 Sep 27; 91(20):9612-6. PMID: 7937815.
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    16. Huttenlocher PR, Taravath S, Mojtahedi S. Periventricular heterotopia and epilepsy. Neurology. 1994 Jan; 44(1):51-5. PMID: 8290091.
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    17. Roach ES, Smith M, Huttenlocher P, Bhat M, Alcorn D, Hawley L. Diagnostic criteria: tuberous sclerosis complex. Report of the Diagnostic Criteria Committee of the National Tuberous Sclerosis Association. J Child Neurol. 1992 Apr; 7(2):221-4. PMID: 1573244.
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    18. Pavone L, Huttenlocher P, Siciliano L, Micali G, Rizzo R, Anastasi M, Maimone D, Woolmann R. Two brothers with a variant of hereditary sensory neuropathy. Neuropediatrics. 1992 Apr; 23(2):92-5. PMID: 1376446.
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    19. Berry-Kravis E, Huttenlocher PR. Cyclic AMP metabolism in fragile X syndrome. Ann Neurol. 1992 Jan; 31(1):22-6. PMID: 1371909.
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    20. Huttenlocher PR, Bonnier C. Effects of changes in the periphery on development of the corticospinal motor system in the rat. Brain Res Dev Brain Res. 1991 Jun 21; 60(2):253-60. PMID: 1893567.
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    21. Huttenlocher PR. Dendritic and synaptic pathology in mental retardation. Pediatr Neurol. 1991 Mar-Apr; 7(2):79-85. PMID: 2059260.
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    22. Huttenlocher PR, Wollmann RL. Cellular neuropathology of tuberous sclerosis. Ann N Y Acad Sci. 1991; 615:140-8. PMID: 2039139.
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    23. Huttenlocher PR, Hapke RJ. A follow-up study of intractable seizures in childhood. Ann Neurol. 1990 Nov; 28(5):699-705. PMID: 2260857.
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    24. Huttenlocher PR, Levine SC, Huttenlocher J, Gates J. Discrimination of normal and at-risk preschool children on the basis of neurological tests. Dev Med Child Neurol. 1990 May; 32(5):394-402. PMID: 2354753.
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    25. Huttenlocher PR. Morphometric study of human cerebral cortex development. Neuropsychologia. 1990; 28(6):517-27. PMID: 2203993.
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    26. Banich MT, Levine SC, Kim H, Huttenlocher P. The effects of developmental factors on IQ in hemiplegic children. Neuropsychologia. 1990; 28(1):35-47. PMID: 2314563.
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    27. Kohrman MH, Sugioka C, Huttenlocher PR, Spire JP. Inter- versus intra-subject variance in topographic mapping of the electroencephalogram. Clin Electroencephalogr. 1989 Oct; 20(4):248-53. PMID: 2791314.
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    28. Huttenlocher PR, Raichelson RM. Effects of neonatal hemispherectomy on location and number of corticospinal neurons in the rat. Brain Res Dev Brain Res. 1989 May 01; 47(1):59-69. PMID: 2472235.
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    29. Hong-Magno ET, Muraki AS, Huttenlocher PR. Atypical CT scans in adrenoleukodystrophy. J Comput Assist Tomogr. 1987 Mar-Apr; 11(2):333-6. PMID: 3819136.
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    30. Levine SC, Huttenlocher P, Banich MT, Duda E. Factors affecting cognitive functioning of hemiplegic children. Dev Med Child Neurol. 1987 Feb; 29(1):27-35. PMID: 3556798.
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    31. Amarose AP, Huttenlocher PR, Sprudzs RM, Laitsch TJ, Pettenati MJ. A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome. Hum Genet. 1987 Jan; 75(1):4-6. PMID: 3804330.
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    32. Huttenlocher PR, de Courten C. The development of synapses in striate cortex of man. Hum Neurobiol. 1987; 6(1):1-9. PMID: 3583840.
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    33. Cashman NR, Antel JP, Hancock LW, Dawson G, Horwitz AL, Johnson WG, Huttenlocher PR, Wollmann RL. N-acetyl-beta-hexosaminidase beta locus defect and juvenile motor neuron disease: a case study. Ann Neurol. 1986 Jun; 19(6):568-72. PMID: 3014997.
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    34. Kohrman MH, Huttenlocher PR. Takayasu arteritis: a treatable cause of stroke in infancy. Pediatr Neurol. 1986 May-Jun; 2(3):154-8. PMID: 2907858.
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    35. Huttenlocher PR, Picchietti DL, Roos RP, Cashman NR, Horowitz B, Horowitz MS. Intrathecal interferon in subacute sclerosing panencephalitis. Ann Neurol. 1986 Mar; 19(3):303-5. PMID: 2421637.
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    36. Jacobsen JH, Rosenberg RS, Huttenlocher PR, Spire JP. Familial nocturnal cramping. Sleep. 1986; 9(1):54-60. PMID: 3961367.
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    37. Huttenlocher PR, Heydemann PT. Fine structure of cortical tubers in tuberous sclerosis: a Golgi study. Ann Neurol. 1984 Nov; 16(5):595-602. PMID: 6508241.
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    38. Huttenlocher PR. Reye's syndrome--still an elusive entity. West J Med. 1984 Aug; 141(2):236-7. PMID: 6495728.
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    39. Huttenlocher PR, Moohr JW, Johns L, Brown FD. Cerebral blood flow in sickle cell cerebrovascular disease. Pediatrics. 1984 May; 73(5):615-21. PMID: 6718116.
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    40. Huttenlocher PR. Synapse elimination and plasticity in developing human cerebral cortex. Am J Ment Defic. 1984 Mar; 88(5):488-96. PMID: 6731486.
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    41. Huttenlocher PR, de Courten C, Garey LJ, Van der Loos H. Synaptogenesis in human visual cortex--evidence for synapse elimination during normal development. Neurosci Lett. 1982 Dec 13; 33(3):247-52. PMID: 7162689.
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    42. Jones CE, Dyken PR, Huttenlocher PR, Jabbour JT, Maxwell KW. Inosiplex therapy in subacute sclerosing panencephalitis. A multicentre, non-randomised study in 98 patients. Lancet. 1982 May 08; 1(8280):1034-7. PMID: 6176821.
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    43. Huttenlocher PR, De Courten C, Garey LJ, Van der Loos H. Synaptic development in human cerebral cortex. Int J Neurol. 1982-1983; 16-17:144-54. PMID: 6765658.
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    44. Tonsgard JH, Huttenlocher PR, Thisted RA. Lactic acidemia in Reye's syndrome. Pediatrics. 1982 Jan; 69(1):64-9. PMID: 7054762.
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    45. Tonsgard JH, Huttenlocher PR. Salicylates and Reye's syndrome. Pediatrics. 1981 Nov; 68(5):747-8. PMID: 7312481.
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    46. Ehrenberg M, Tripathi RC, Wollman RL, Huttenlocher PR, Johnson RO, McCoy FE. Pigmentary macular degeneration with multifocal necrotizing encephalopathy. Am J Ophthalmol. 1981 Sep; 92(3):422-30. PMID: 7294103.
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    47. Garber BB, Huttenlocher PR, Larramendi LH. Self-assembly of cortical plate cells in vitro within embryonic mouse cerebral aggregates. Golgi and electron microscopic analysis. Brain Res. 1980 Nov 17; 201(2):255-78. PMID: 7417843.
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    48. Huttenlocher PR. Natural course of febrile seizures. Pediatrics. 1980 Mar; 65(3):680. PMID: 7360574.
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    49. Duda EE, Huttenlocher PR, Patronas NJ. CT of subacute sclerosing panencephalitis. AJNR Am J Neuroradiol. 1980 Jan-Feb; 1(1):35-8. PMID: 6779587.
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    50. Amarose AP, Dorus E, Huttenlocher PR, Csaszar S. A ring 14 chromosome with deleted short arm. Hum Genet. 1980; 54(2):145-7. PMID: 6156115.
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    51. Newell FW, Johnson RO, Huttenlocher PR. Pigmentary degeneration of the retina in the Hallervorden-Spatz syndrome. Am J Ophthalmol. 1979 Sep; 88(3 Pt 1):467-71. PMID: 573556.
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    52. Chelmicka-Schorr E, Bernstein LP, Zurbrugg EB, Huttenlocher PR. Eaton-Lambert syndrome in a 9-year-old girl. Arch Neurol. 1979 Sep; 36(9):572-4. PMID: 475622.
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    53. Huttenlocher PR, Mattson RH. Isoprinosine in subacute sclerosing panencephalitis. Neurology. 1979 Jun; 29(6):763-71. PMID: 88024.
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    54. Huttenlocher PR. Synaptic density in human frontal cortex - developmental changes and effects of aging. Brain Res. 1979 Mar 16; 163(2):195-205. PMID: 427544.
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    55. Trauner DA, Brown F, Ganz E, Huttenlocher PR. Treatment of elevated intracranial pressure in Reye syndrome. Ann Neurol. 1978 Sep; 4(3):275-8. PMID: 718141.
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    56. Trauner DA, Huttenlocher PR. Short chain fatty acid-induced central hyperventilation in rabbits. Neurology. 1978 Sep; 28(9 Pt 1):940-4. PMID: 567765.
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    57. Huttenlocher PR, Trauner DA. Reye's syndrome in infancy. Pediatrics. 1978 Jul; 62(1):84-90. PMID: 683788.
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    58. Huttenlocher PR, Amemiya IM. Effects of adrenocortical steroids and of adrenocorticotrophic hormone on (Na+-K+)-ATPase in immature cerebral cortex. Pediatr Res. 1978 Feb; 12(2):104-7. PMID: 205825.
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    59. Duda EE, Huttenlocher PR. Computed tomography in adrenoleukodystrophy. Correlation of radiological and histological findings. Radiology. 1976 Aug; 120(2):349-50. PMID: 778911.
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    60. Huttenlocher PR. Ketonemia and seizures: metabolic and anticonvulsant effects of two ketogenic diets in childhood epilepsy. Pediatr Res. 1976 May; 10(5):536-40. PMID: 934725.
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    61. Huttenlocher PR, Solitare GB, Adams G. Infantile diffuse cerebral degeneration with hepatic cirrhosis. Arch Neurol. 1976 Mar; 33(3):186-92. PMID: 1252162.
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    62. Snead OC, Yu RK, Huttenlocher PR. Gamma hydroxybutyrate. Correlation of serum and cerebrospinal fluid levels with electroencephalographic and behavioral effects. Neurology. 1976 Jan; 26(1):51-6. PMID: 942770.
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    63. Snead OC, Kier EL, Huttenlocher PR. Unilateral nerve deafness in childhood: a possible vascular etiology. Dev Med Child Neurol. 1975 Feb; 17(1):84-8. PMID: 1123124.
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    64. Huttenlocher PR. Snyaptic and dendritic development and mental defect. UCLA Forum Med Sci. 1975; (18):123-40. PMID: 1198709.
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    65. Oda MA, Huttenlocher PR. The effect of corticosteroids on dendritic development in the rat brain. Yale J Biol Med. 1974 Sep; 47(3):155-65. PMID: 4446628.
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    66. Huttenlocher PR. Dendritic development in neocortex of children with mental defect and infantile spasms. Neurology. 1974 Mar; 24(3):203-10. PMID: 4130661.
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    67. Huttenlocher PR, Huttenlocher J. A study of children with hyperlexia. Neurology. 1973 Oct; 23(10):1107-16. PMID: 4795424.
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    68. Gumbinas M, Oda M, Huttenlocher P. The effects of corticosteroids on myelination of the developing rat brain. Biol Neonate. 1973; 22(5):355-66. PMID: 4778314.
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    69. Yogman MW, Speroff L, Huttenlocher PR, Kase NG. Child development after pregnancies complicated by low urinary estriol excretion and pre-eclampsia. Am J Obstet Gynecol. 1972 Dec 15; 114(8):1069-77. PMID: 4635202.
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    70. Huttenlocher PR. Reye's syndrome: relation of outcome to therapy. J Pediatr. 1972 May; 80(5):845-50. PMID: 5018398.
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    71. Huttenlocher PR, Wilbourn AJ, Signore JM. Medium-chain triglycerides as a therapy for intractable childhood epilepsy. Neurology. 1971 Nov; 21(11):1097-103. PMID: 5166216.
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    72. Huttenlocher PR. Myelination and the development of function in immature pyramidal tract. Exp Neurol. 1970 Dec; 29(3):405-15. PMID: 5492915.
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    73. Huttenlocher PR, Hillman RE, Hsia YE. Pseudotumor cerebri in galactosemia. J Pediatr. 1970 Jun; 76(6):902-5. PMID: 5444582.
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    74. Huttenlocher PR. Dendritic development and mental defect. Neurology. 1970 Apr; 20(4):381. PMID: 5534993.
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    75. Huttenlocher PR, Landwirth J, Hanson V, Gallagher BB, Bensch K. Osteo-chondro-muscular dystrophy. A disorder manifested by multiple skeletal deformities, myotonia, and dystrophic changes in muscle. Pediatrics. 1969 Dec; 44(6):945-58. PMID: 5365059.
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    76. Huttenlocher PR, Schwartz AD, Klatskin G. Reye's syndrome: ammonia intoxication as a possible factor in the encephalopathy. Pediatrics. 1969 Mar; 43(3):443-54. PMID: 5812402.
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    77. Herman MM, Huttenlocher PR, Bensch KG. Electron microscopic observations in infantile neuroaxonal dystrophy. Report of a cortical biopsy and review of the recent literature. Arch Neurol. 1969 Jan; 20(1):19-34. PMID: 4179165.
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    78. Huttenlocher PR, Smith DB. Acute infantile hemiplegia associated with thrombocytosis. Dev Med Child Neurol. 1968 Oct; 10(5):621-5. PMID: 5708281.
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    79. Huttenlocher PR, Rawson MD. Neurfnal activity and adenosine triphosphatase in immature cerebral cortex. Exp Neurol. 1968 Sep; 22(1):118-29. PMID: 4235007.
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    80. Huttenlocher PR, Gilles FH. Infantile neuroaxonal dystrophy. Clinical, pathologic, and histochemical findings in a family with 3 affected siblings. Neurology. 1967 Dec; 17(12):1174-84. PMID: 6070019.
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    81. Ciccarelli EC, Huttenlocher PR. Diencephalic tumor. A cause of infantile nystagmus and cachexia. Arch Ophthalmol. 1967 Sep; 78(3):350-3. PMID: 5298708.
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    82. Huttenlocher PR. Development of cortical neuronal activity in the neonatal cat. Exp Neurol. 1967 Mar; 17(3):247-62. PMID: 6019258.
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    83. Huttenlocher PR. Development of neuronal activity in neocortex of the kitten. Nature. 1966 Jul 02; 211(5044):91-2. PMID: 5967481.
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    84. Huttenlocher PR, Cohen RB. Oxidative enzymes in spinal motor neurons in Werdnig-Hoffmann disease. A comparison with the axonal reaction. Neurology. 1966 Apr; 16(4):398-406. PMID: 5948648.
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    85. HUTTENLOCHER PR. TREATMENT OF HYDROCEPHALUS WITH ACETAZOLAMIDE: RESULTS IN 15 CASES. J Pediatr. 1965 Jun; 66:1023-30. PMID: 14288454.
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    86. HUTTENLOCHER PR. Accidental glutethimide intoxication in children. N Engl J Med. 1963 Jul 04; 269:38-9. PMID: 13955953.
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    87. EVARTS EV, BENTAL E, BIHARI B, HUTTENLOCHER PR. Spontaneous discharge of single neurons during sleep and waking. Science. 1962 Mar 02; 135(3505):726-8. PMID: 13891034.
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    88. HUTTENLOCHER PR. Effects of state of arousal on click responses in the mesencephalic reticular formation. Electroencephalogr Clin Neurophysiol. 1960 Nov; 12:819-27. PMID: 13717086.
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    89. EVARTS EV, FLEMING TC, HUTTENLOCHER PR. Recovery cycle of visual cortex of the awake and sleeping cat. Am J Physiol. 1960 Aug; 199:373-6. PMID: 13697614.
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