| Year |
Citation |
Score |
| 2013 |
Fanous AA, Quigley EP, Chin SS, Couldwell WT. Giant necrotic pituitary apoplexy. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 20: 1462-4. PMID 23623615 DOI: 10.1016/J.Jocn.2012.07.023 |
0.318 |
|
| 2011 |
Selcen D, Bromberg MB, Chin SS, Engel AG. Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy. Neurology. 77: 1951-9. PMID 22094483 DOI: 10.1212/Wnl.0B013E31823A0Ebe |
0.301 |
|
| 2011 |
Niazi TN, Shah LM, Chin SS, Schmidt MH. Isolated intradural lumbosacral tailgut cyst with carcinoid features. Journal of Neurosurgery. Spine. 14: 382-7. PMID 21250817 DOI: 10.3171/2010.11.Spine09763 |
0.329 |
|
| 2011 |
Mumert ML, Walsh MT, Chin SS, Couldwell WT. Cystic granular cell tumor mimicking Rathke cleft cyst. Journal of Neurosurgery. 114: 325-8. PMID 20509726 DOI: 10.3171/2010.5.Jns1058 |
0.353 |
|
| 2010 |
Sayama CM, Osborn AG, Chin SS, Couldwell WT. Capillary telangiectasias: clinical, radiographic, and histopathological features. Clinical article. Journal of Neurosurgery. 113: 709-14. PMID 19817536 DOI: 10.3171/2009.9.Jns09282 |
0.315 |
|
| 2009 |
Schessl J, Taratuto AL, Sewry C, Battini R, Chin SS, Maiti B, Dubrovsky AL, Erro MG, Espada G, Robertella M, Saccoliti M, Olmos P, Bridges LR, Standring P, Hu Y, et al. Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1. Brain : a Journal of Neurology. 132: 452-64. PMID 19181672 DOI: 10.1093/Brain/Awn325 |
0.352 |
|
| 2009 |
Comstock JM, Bruggers C, Moser K, Hedlund G, Chin S, Riva-Cambrin J, Zhou H. Leptomeningeal melanoma with foci of rhabdomyosarcoma in an infant with giant congenital nevi: A case report and literature review Pathology Case Reviews. 14: 100-103. DOI: 10.1097/Pcr.0B013E3181A6E400 |
0.352 |
|
| 2008 |
Bishop FS, Liu JK, Chin SS, Fults DW. Recurrent cerebellar hemangioblastoma with enhancing tumor in the cyst wall: case report. Neurosurgery. 62: E1378-9; discussion . PMID 18824960 DOI: 10.1227/01.Neu.0000316430.77623.35 |
0.336 |
|
| 2008 |
Linscott LL, Osborn AG, Blaser S, Castillo M, Hewlett RH, Wieselthaler N, Chin SS, Krakenes J, Hedlund GL, Sutton CL. Pilomyxoid astrocytoma: expanding the imaging spectrum. Ajnr. American Journal of Neuroradiology. 29: 1861-6. PMID 18701580 DOI: 10.3174/Ajnr.A1233 |
0.327 |
|
| 2008 |
Mehta LR, Huddleston BJ, Skalabrin EJ, Burns JB, Zou WQ, Gambetti P, Chin SS. Sporadic fatal insomnia masquerading as a paraneoplastic cerebellar syndrome. Archives of Neurology. 65: 971-3. PMID 18625868 DOI: 10.1001/Archneur.65.7.971 |
0.376 |
|
| 2008 |
Schessl J, Zou Y, McGrath MJ, Cowling BS, Maiti B, Chin SS, Sewry C, Battini R, Hu Y, Cottle DL, Rosenblatt M, Spruce L, Ganguly A, Kirschner J, Judkins AR, et al. Proteomic identification of FHL1 as the protein mutated in human reducing body myopathy. The Journal of Clinical Investigation. 118: 904-12. PMID 18274675 DOI: 10.1172/Jci34450 |
0.305 |
|
| 2007 |
Gottfried ON, Chin S, Davidson HC, Couldwell WT. Trigeminal amyloidoma: case report and review of the literature. Skull Base : Official Journal of North American Skull Base Society ... [Et Al.]. 17: 317-24. PMID 18330430 DOI: 10.1055/S-2007-986430 |
0.329 |
|
| 2007 |
Liu JK, Sayama C, Chin SS, Couldwell WT. Extranodal NK/T-cell lymphoma presenting as a pituitary mass. Case report and review of the literature. Journal of Neurosurgery. 107: 660-5. PMID 17886569 DOI: 10.3171/Jns-07/09/0660 |
0.33 |
|
| 2007 |
Sampson JB, Smith SM, Smith AG, Singleton JR, Chin S, Pestronk A, Flanigan KM. Paraneoplastic myopathy: response to intravenous immunoglobulin. Neuromuscular Disorders : Nmd. 17: 404-8. PMID 17336069 DOI: 10.1016/J.Nmd.2007.01.004 |
0.315 |
|
| 2007 |
Bell JW, Osborn AG, Salzman KL, Blaser SI, Jones BV, Chin SS. Neuroradiologic characteristics of astroblastoma. Neuroradiology. 49: 203-9. PMID 17216265 DOI: 10.1007/S00234-006-0182-0 |
0.34 |
|
| 2007 |
Amini A, Chin SS, Schmidt MH. Malignant transformation of conus medullaris ganglioglioma: case report. Journal of Neuro-Oncology. 82: 313-5. PMID 17151931 DOI: 10.1007/S11060-006-9288-9 |
0.351 |
|
| 2006 |
Opitz JM, Putnam AR, Comstock JM, Chin S, Byrne JLB, Kennedy A, Frikke MJ, Bernard C, Albrecht S, Kaloustian VD, Szakacs JG. Mortality and pathological findings in C (Opitz trigonocephaly) syndrome Fetal and Pediatric Pathology. 25: 211-231. PMID 17162528 DOI: 10.1080/15513810601015753 |
0.316 |
|
| 2006 |
Sampson JB, Chin SS, Clayton FC, Pestronk A, Swoboda KJ, Flanigan KM. An unusual pathologic feature associated with dermatomyositis. Neuromuscular Disorders : Nmd. 16: 391-3. PMID 16697198 DOI: 10.1016/J.Nmd.2006.03.013 |
0.339 |
|
| 2006 |
Amini A, Schmidt RH, Salzman KL, Chin SS, Couldwell WT. Glioblastoma multiforme of the pineal region. Journal of Neuro-Oncology. 79: 307-14. PMID 16645719 DOI: 10.1007/S11060-006-9145-X |
0.355 |
|
| 2006 |
McCall T, Chin SS, Salzman KL, Fults DW. Tuberous sclerosis: a syndrome of incomplete tumor suppression. Neurosurgical Focus. 20: E3. PMID 16459993 DOI: 10.3171/Foc.2006.20.1.4 |
0.364 |
|
| 2005 |
Pastore M, Chin SS, Bell KL, Dong Z, Yang Q, Yang L, Yuan J, Chen SG, Gambetti P, Zou WQ. Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: relationship with sporadic CJD. The American Journal of Pathology. 167: 1729-38. PMID 16314483 DOI: 10.1016/S0002-9440(10)61254-0 |
0.309 |
|
| 2004 |
Gordon PH, Fahn S, Chin S, Golbe LI, Lynch T, Eidelberg D. Woman with a 26-year history of parkinsonism, supranuclear ophthalmoplegia, and loss of postural reflexes. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 950-61. PMID 15300663 DOI: 10.1002/Mds.20139 |
0.313 |
|
| 2004 |
Kulikova-Schupak R, Knupp KG, Pascual JM, Chin SS, Kairam R, Patterson MC. Rectal biopsy in the diagnosis of neuronal intranuclear hyaline inclusion disease. Journal of Child Neurology. 19: 59-62. PMID 15032387 DOI: 10.1177/08830738040190010707 |
0.312 |
|
| 2003 |
Rippon GA, Crook R, Baker M, Halvorsen E, Chin S, Hutton M, Houlden H, Hardy J, Lynch T. Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia. Archives of Neurology. 60: 884-8. PMID 12810495 DOI: 10.1001/Archneur.60.6.884 |
0.313 |
|
| 1999 |
Worrall BB, Herman ST, Capellari S, Lynch T, Chin S, Gambetti P, Parchi P. Type 1 protease resistant prion protein and valine homozygosity at codon 129 of PRNP identify a subtype of sporadic Creutzfeldt-Jakob disease. Journal of Neurology, Neurosurgery, and Psychiatry. 67: 671-4. PMID 10519879 DOI: 10.1136/Jnnp.67.5.671 |
0.305 |
|
| 1999 |
Parchi P, Capellari S, Chin S, Schwarz HB, Schecter NP, Butts JD, Hudkins P, Burns DK, Powers JM, Gambetti P. A subtype of sporadic prion disease mimicking fatal familial insomnia. Neurology. 52: 1757-63. PMID 10371520 DOI: 10.1212/Wnl.52.9.1757 |
0.328 |
|
| 1999 |
Desmond DW, Moroney JT, Lynch T, Chan S, Chin SS, Mohr JP. The natural history of CADASIL: a pooled analysis of previously published cases. Stroke; a Journal of Cerebral Circulation. 30: 1230-3. PMID 10356105 DOI: 10.1161/01.Str.30.6.1230 |
0.313 |
|
| 1998 |
Chan S, Chin SS, Nordli DR, Goodman RR, DeLaPaz RL, Pedley TA. Prospective magnetic resonance imaging identification of focal cortical dysplasia, including the non-balloon cell subtype. Annals of Neurology. 44: 749-57. PMID 9818930 DOI: 10.1002/Ana.410440508 |
0.328 |
|
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