The efficacy of adrenocorticotropic hormone in a girl with anti-N-methyl-D-aspartate receptor encephalitis
Immunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we describe the use of adrenocorticotropic hormone (ACTH) immunotherapy with good outcome in a patient with anti-NMDAR encephalitis. A 4-year-ol...
Saved in:
Published in | Brain & development (Tokyo. 1979) Vol. 40; no. 3; pp. 247 - 250 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.03.2018
|
Subjects | |
Online Access | Get full text |
ISSN | 0387-7604 1872-7131 1872-7131 |
DOI | 10.1016/j.braindev.2017.10.003 |
Cover
Abstract | Immunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we describe the use of adrenocorticotropic hormone (ACTH) immunotherapy with good outcome in a patient with anti-NMDAR encephalitis.
A 4-year-old girl developed convulsions in her right arm and leg without impaired consciousness. These convulsions occurred frequently in clusters of 10–20 events of 10–20 s duration. She was admitted to our hospital on the 6th day following her initial series of convulsions. Flaccid paralysis of the right hand and leg was also found. Interictal electroencephalography showed high-amplitude slow waves. No abnormal findings were shown on MRI. 99mTc-ECD brain SPECT on the 14th day showed hyperperfusion in the left hemisphere, including the left basal ganglia. The convulsions ceased following the oral administration of valproic acid on the 10th day; however, paralysis associated with choreic dyskinesia of the right arm and leg remained. ACTH immunotherapy was then performed on the 15th day. We identified the presence of N-methyl-D-aspartate receptor antibody in CSF samples taken on the 6th day. After ACTH therapy, the patient fully recovered from the paralysis associated with choreic dyskinesia of the right arm and leg. She has not had a relapse and has not required medication for over a year.
ACTH immunotherapy may be a useful treatment option for patients with anti-NMDAR encephalitis, although further evaluation is required. |
---|---|
AbstractList | Immunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we describe the use of adrenocorticotropic hormone (ACTH) immunotherapy with good outcome in a patient with anti-NMDAR encephalitis.BACKGROUNDImmunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we describe the use of adrenocorticotropic hormone (ACTH) immunotherapy with good outcome in a patient with anti-NMDAR encephalitis.A 4-year-old girl developed convulsions in her right arm and leg without impaired consciousness. These convulsions occurred frequently in clusters of 10-20 events of 10-20 s duration. She was admitted to our hospital on the 6th day following her initial series of convulsions. Flaccid paralysis of the right hand and leg was also found. Interictal electroencephalography showed high-amplitude slow waves. No abnormal findings were shown on MRI. 99mTc-ECD brain SPECT on the 14th day showed hyperperfusion in the left hemisphere, including the left basal ganglia. The convulsions ceased following the oral administration of valproic acid on the 10th day; however, paralysis associated with choreic dyskinesia of the right arm and leg remained. ACTH immunotherapy was then performed on the 15th day. We identified the presence of N-methyl-D-aspartate receptor antibody in CSF samples taken on the 6th day. After ACTH therapy, the patient fully recovered from the paralysis associated with choreic dyskinesia of the right arm and leg. She has not had a relapse and has not required medication for over a year.SUBJECT AND METHODSA 4-year-old girl developed convulsions in her right arm and leg without impaired consciousness. These convulsions occurred frequently in clusters of 10-20 events of 10-20 s duration. She was admitted to our hospital on the 6th day following her initial series of convulsions. Flaccid paralysis of the right hand and leg was also found. Interictal electroencephalography showed high-amplitude slow waves. No abnormal findings were shown on MRI. 99mTc-ECD brain SPECT on the 14th day showed hyperperfusion in the left hemisphere, including the left basal ganglia. The convulsions ceased following the oral administration of valproic acid on the 10th day; however, paralysis associated with choreic dyskinesia of the right arm and leg remained. ACTH immunotherapy was then performed on the 15th day. We identified the presence of N-methyl-D-aspartate receptor antibody in CSF samples taken on the 6th day. After ACTH therapy, the patient fully recovered from the paralysis associated with choreic dyskinesia of the right arm and leg. She has not had a relapse and has not required medication for over a year.ACTH immunotherapy may be a useful treatment option for patients with anti-NMDAR encephalitis, although further evaluation is required.CONCLUSIONACTH immunotherapy may be a useful treatment option for patients with anti-NMDAR encephalitis, although further evaluation is required. Immunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we describe the use of adrenocorticotropic hormone (ACTH) immunotherapy with good outcome in a patient with anti-NMDAR encephalitis. A 4-year-old girl developed convulsions in her right arm and leg without impaired consciousness. These convulsions occurred frequently in clusters of 10–20 events of 10–20 s duration. She was admitted to our hospital on the 6th day following her initial series of convulsions. Flaccid paralysis of the right hand and leg was also found. Interictal electroencephalography showed high-amplitude slow waves. No abnormal findings were shown on MRI. 99mTc-ECD brain SPECT on the 14th day showed hyperperfusion in the left hemisphere, including the left basal ganglia. The convulsions ceased following the oral administration of valproic acid on the 10th day; however, paralysis associated with choreic dyskinesia of the right arm and leg remained. ACTH immunotherapy was then performed on the 15th day. We identified the presence of N-methyl-D-aspartate receptor antibody in CSF samples taken on the 6th day. After ACTH therapy, the patient fully recovered from the paralysis associated with choreic dyskinesia of the right arm and leg. She has not had a relapse and has not required medication for over a year. ACTH immunotherapy may be a useful treatment option for patients with anti-NMDAR encephalitis, although further evaluation is required. Immunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we describe the use of adrenocorticotropic hormone (ACTH) immunotherapy with good outcome in a patient with anti-NMDAR encephalitis. A 4-year-old girl developed convulsions in her right arm and leg without impaired consciousness. These convulsions occurred frequently in clusters of 10-20 events of 10-20 s duration. She was admitted to our hospital on the 6th day following her initial series of convulsions. Flaccid paralysis of the right hand and leg was also found. Interictal electroencephalography showed high-amplitude slow waves. No abnormal findings were shown on MRI. Tc-ECD brain SPECT on the 14th day showed hyperperfusion in the left hemisphere, including the left basal ganglia. The convulsions ceased following the oral administration of valproic acid on the 10th day; however, paralysis associated with choreic dyskinesia of the right arm and leg remained. ACTH immunotherapy was then performed on the 15th day. We identified the presence of N-methyl-D-aspartate receptor antibody in CSF samples taken on the 6th day. After ACTH therapy, the patient fully recovered from the paralysis associated with choreic dyskinesia of the right arm and leg. She has not had a relapse and has not required medication for over a year. ACTH immunotherapy may be a useful treatment option for patients with anti-NMDAR encephalitis, although further evaluation is required. |
Author | Okumura, Akihisa Natsume, Jun Nomura, Shohei Shimakawa, Shuichi Kashiwagi, Mitsuru Tamai, Hiroshi Hatanaka, Mari Fukui, Miho |
Author_xml | – sequence: 1 givenname: Mari surname: Hatanaka fullname: Hatanaka, Mari organization: Department of Pediatrics, Osaka Medical College, Osaka, Japan – sequence: 2 givenname: Shuichi surname: Shimakawa fullname: Shimakawa, Shuichi email: ZVQ10523@nifty.com organization: Department of Pediatrics, Osaka Medical College, Osaka, Japan – sequence: 3 givenname: Akihisa surname: Okumura fullname: Okumura, Akihisa organization: Department of Pediatrics, Aichi Medical University, Aichi, Japan – sequence: 4 givenname: Jun surname: Natsume fullname: Natsume, Jun organization: Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan – sequence: 5 givenname: Miho surname: Fukui fullname: Fukui, Miho organization: Department of Pediatrics, Osaka Medical College, Osaka, Japan – sequence: 6 givenname: Shohei surname: Nomura fullname: Nomura, Shohei organization: Department of Pediatrics, Hirakata Municipal Hospital, Osaka, Japan – sequence: 7 givenname: Mitsuru surname: Kashiwagi fullname: Kashiwagi, Mitsuru organization: Department of Pediatrics, Hirakata Municipal Hospital, Osaka, Japan – sequence: 8 givenname: Hiroshi surname: Tamai fullname: Tamai, Hiroshi organization: Department of Pediatrics, Osaka Medical College, Osaka, Japan |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29122401$$D View this record in MEDLINE/PubMed |
BookMark | eNqNkU9v1DAQxS1URLeFr1D5yCXbsfPHyQWBChSkil7as-W1x8RLYgfbW7TfHq-25cClvcyMRm-e5fc7Iyc-eCTkgsGaAesut-tNVM4bfFhzYKIs1wD1K7JiveCVYDU7ISuoe1GJDppTcpbSFgAYZ_CGnPKBcd4AW5Ht3YgUrXVa6T0NlioT0QcdYnY65BgWp-kY4lyep85TRX-6ONE_Lo9U-eyqH9WMedxP1edKpUXFrDLSiBqXHCJFX4ZRTS679Ja8tmpK-O6xn5P7r1_urr5VN7fX368-3VS6HppcKWtsW4rqTNdrYzuAnreDaNqOmzLrptmIXg9g2QDQciXqflADWs4sb6yuz8n7o-8Sw-8dpixnlzROk_IYdkmyoau5YKLti_TiUbrbzGjkEt2s4l4-5VME3VGgY0gpov0nYSAPIORWPoGQBxCHfQFRDj8eD7H89MFhlEm7QxrGlXCyNME9b_HhPws9OV9ATb9w_xKDv7uuqlE |
Cites_doi | 10.1016/j.autrev.2012.03.001 10.1001/jamaneurol.2014.2956 10.3389/fneur.2013.00021 10.1016/S1474-4422(12)70310-1 10.1016/j.braindev.2015.11.007 10.1177/0883073813515947 10.1186/1742-2094-10-10 10.1016/j.jpeds.2009.07.048 10.1016/j.jpeds.2012.10.011 10.1177/0883073812469054 |
ContentType | Journal Article |
Copyright | 2017 The Japanese Society of Child Neurology Copyright © 2017 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved. |
Copyright_xml | – notice: 2017 The Japanese Society of Child Neurology – notice: Copyright © 2017 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved. |
DBID | AAYXX CITATION NPM 7X8 |
DOI | 10.1016/j.braindev.2017.10.003 |
DatabaseName | CrossRef PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef PubMed MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic PubMed |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1872-7131 |
EndPage | 250 |
ExternalDocumentID | 29122401 10_1016_j_braindev_2017_10_003 S0387760417302681 |
Genre | Journal Article |
GroupedDBID | --- --K --M .1- .55 .FO .GJ .~1 0R~ 1B1 1P~ 1RT 1~. 1~5 23N 3O- 4.4 457 4G. 53G 5GY 5RE 5VS 6J9 7-5 71M 8P~ 9JM AABNK AAEDT AAEDW AAIKJ AAKOC AALRI AAOAW AAQFI AAQXK AATTM AAXKI AAXLA AAXUO AAYWO ABBQC ABCQJ ABFNM ABFRF ABIVO ABJNI ABMAC ABMZM ABTEW ABWVN ABXDB ACDAQ ACGFO ACGFS ACIEU ACIUM ACRLP ACRPL ACVFH ADBBV ADCNI ADEZE ADMUD ADNMO AEBSH AEFWE AEIPS AEKER AENEX AEUPX AEVXI AFJKZ AFPUW AFRHN AFTJW AFXIZ AGCQF AGHFR AGQPQ AGUBO AGWIK AGYEJ AHHHB AIEXJ AIGII AIIUN AIKHN AITUG AJRQY AJUYK AKBMS AKRLJ AKRWK AKYEP ALMA_UNASSIGNED_HOLDINGS AMRAJ ANKPU ANZVX APXCP ASPBG AVWKF AXJTR AZFZN BKOJK BLXMC BNPGV CS3 DU5 EBS EFJIC EFKBS EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU FYGXN G-2 G-Q GBLVA HDW HMK HMO HMQ HVGLF HZ~ IHE J1W KOM LX8 M29 M2V M41 MO0 MOBAO N9A O-L O9- OAUVE OP~ OZT P-8 P-9 P2P PC. Q38 R2- ROL RPZ SAE SCC SDF SDG SDP SEL SES SEW SNS SPCBC SSH SSN SSZ T5K UNMZH WUQ X7M Z5R ZGI ~G- AACTN AADPK AAIAV ABLVK ABYKQ AFCTW AFKWA AHPSJ AJBFU AJOXV AMFUW EFLBG LCYCR RIG AAYXX AGRNS CITATION NPM 7X8 |
ID | FETCH-LOGICAL-c394t-afdf5afda6d68cdf600825974562d008c44b78c90f190052a7389a9ef21f24fc3 |
IEDL.DBID | AIKHN |
ISSN | 0387-7604 1872-7131 |
IngestDate | Thu Sep 04 18:52:04 EDT 2025 Wed Feb 19 02:43:28 EST 2025 Tue Jul 01 03:19:45 EDT 2025 Fri Feb 23 02:32:47 EST 2024 Tue Aug 26 16:34:15 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 3 |
Keywords | Treatment ACTH therapy Autoimmune focal encephalitis Anti-N-methyl-D-aspartate receptor encephalitis |
Language | English |
License | Copyright © 2017 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c394t-afdf5afda6d68cdf600825974562d008c44b78c90f190052a7389a9ef21f24fc3 |
Notes | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
PMID | 29122401 |
PQID | 1963271758 |
PQPubID | 23479 |
PageCount | 4 |
ParticipantIDs | proquest_miscellaneous_1963271758 pubmed_primary_29122401 crossref_primary_10_1016_j_braindev_2017_10_003 elsevier_sciencedirect_doi_10_1016_j_braindev_2017_10_003 elsevier_clinicalkey_doi_10_1016_j_braindev_2017_10_003 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | March 2018 2018-03-00 2018-Mar 20180301 |
PublicationDateYYYYMMDD | 2018-03-01 |
PublicationDate_xml | – month: 03 year: 2018 text: March 2018 |
PublicationDecade | 2010 |
PublicationPlace | Netherlands |
PublicationPlace_xml | – name: Netherlands |
PublicationTitle | Brain & development (Tokyo. 1979) |
PublicationTitleAlternate | Brain Dev |
PublicationYear | 2018 |
Publisher | Elsevier B.V |
Publisher_xml | – name: Elsevier B.V |
References | Pranzatelli, Tate (b0045) 2016; 38 Nosadini, Boniver, Zuliani, de Palma, Cainelli, Battistella (b0025) 2015; 30 Peery, Day, Dunn, Fritzler, Prüss, De Souza (b0010) 2012; 11 Sekigawa, Okumura, Niijima, Hayashi, Tanaka, Shimizu (b0015) 2010; 156 Armangue, Titulaer, Málaga, Bataller, Gabilondo, Graus (b0005) 2013; 162 Ross, Ben-Zacharia, Harris, Smrtka (b0030) 2013; 4 Pranzatelli, Tate, McGee, Travelstead, Colliver, Ness (b0040) 2013; 10 Titulaer, McCracken, Gabilondo, Armangué, Glaser, Iizuka (b0020) 2013; 12 Tate, Pranzatelli (b0050) 2013; 28 Leypoldt, Höftberger, Titulaer, Armangue, Gresa-Arribas, Jahn, Rostásy (b0035) 2015; 72 Peery (10.1016/j.braindev.2017.10.003_b0010) 2012; 11 Pranzatelli (10.1016/j.braindev.2017.10.003_b0040) 2013; 10 Sekigawa (10.1016/j.braindev.2017.10.003_b0015) 2010; 156 Leypoldt (10.1016/j.braindev.2017.10.003_b0035) 2015; 72 Armangue (10.1016/j.braindev.2017.10.003_b0005) 2013; 162 Nosadini (10.1016/j.braindev.2017.10.003_b0025) 2015; 30 Pranzatelli (10.1016/j.braindev.2017.10.003_b0045) 2016; 38 Ross (10.1016/j.braindev.2017.10.003_b0030) 2013; 4 Titulaer (10.1016/j.braindev.2017.10.003_b0020) 2013; 12 Tate (10.1016/j.braindev.2017.10.003_b0050) 2013; 28 |
References_xml | – volume: 30 start-page: 238 year: 2015 end-page: 245 ident: b0025 article-title: Longitudinal electroencephalographic (EEG) findings in pediatric anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis: the Padua experience publication-title: J Child Neurol – volume: 156 start-page: 158 year: 2010 end-page: 160 ident: b0015 article-title: Autoimmune focal encephalitis shows marked hypermetabolism on positron emission tomography publication-title: J Pediatr – volume: 12 start-page: 157 year: 2013 end-page: 165 ident: b0020 article-title: Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study publication-title: Lancet Neurol – volume: 38 start-page: 439 year: 2016 end-page: 448 ident: b0045 article-title: Trends and tenets in relapsing and progressive opsoclonus-myoclonus syndrome publication-title: Brain Dev – volume: 72 start-page: 180 year: 2015 end-page: 186 ident: b0035 article-title: Investigations on CXCL13 in anti-N-methyl-D-aspartate receptor encephalitis: a potential biomarker of treatment response publication-title: JAMA Neurol – volume: 10 start-page: 10 year: 2013 ident: b0040 article-title: BAFF/APRIL system in pediatric OMS: relation to severity, neuroinflammation, and immunotherapy publication-title: J Neuroinflam – volume: 28 start-page: 417 year: 2013 end-page: 418 ident: b0050 article-title: Response to correspondence on “active comparator-controlled, rater-blinded study of corticotropin-based immunotherapies for opsoclonus-myoclonus syndrome” publication-title: J Child Neurol – volume: 162 start-page: 850 year: 2013 end-page: 856 ident: b0005 article-title: Pediatric anti-N-methyl-D-aspartate receptor encephalitis-clinical analysis and novel findings in a series of 20 patients publication-title: J Pediatr – volume: 11 start-page: 863 year: 2012 end-page: 872 ident: b0010 article-title: Anti-NMDA receptor encephalitis. The disorder, the diagnosis and the immunobiology publication-title: Autoimmun Rev – volume: 4 start-page: 21 year: 2013 ident: b0030 article-title: Multiple sclerosis, relapses, and the mechanism of action of adrenocorticotropic hormone publication-title: Front Neurol – volume: 11 start-page: 863 year: 2012 ident: 10.1016/j.braindev.2017.10.003_b0010 article-title: Anti-NMDA receptor encephalitis. The disorder, the diagnosis and the immunobiology publication-title: Autoimmun Rev doi: 10.1016/j.autrev.2012.03.001 – volume: 72 start-page: 180 year: 2015 ident: 10.1016/j.braindev.2017.10.003_b0035 article-title: Investigations on CXCL13 in anti-N-methyl-D-aspartate receptor encephalitis: a potential biomarker of treatment response publication-title: JAMA Neurol doi: 10.1001/jamaneurol.2014.2956 – volume: 4 start-page: 21 year: 2013 ident: 10.1016/j.braindev.2017.10.003_b0030 article-title: Multiple sclerosis, relapses, and the mechanism of action of adrenocorticotropic hormone publication-title: Front Neurol doi: 10.3389/fneur.2013.00021 – volume: 12 start-page: 157 year: 2013 ident: 10.1016/j.braindev.2017.10.003_b0020 article-title: Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study publication-title: Lancet Neurol doi: 10.1016/S1474-4422(12)70310-1 – volume: 38 start-page: 439 year: 2016 ident: 10.1016/j.braindev.2017.10.003_b0045 article-title: Trends and tenets in relapsing and progressive opsoclonus-myoclonus syndrome publication-title: Brain Dev doi: 10.1016/j.braindev.2015.11.007 – volume: 30 start-page: 238 year: 2015 ident: 10.1016/j.braindev.2017.10.003_b0025 article-title: Longitudinal electroencephalographic (EEG) findings in pediatric anti-N-methyl-D-aspartate (anti-NMDA) receptor encephalitis: the Padua experience publication-title: J Child Neurol doi: 10.1177/0883073813515947 – volume: 10 start-page: 10 year: 2013 ident: 10.1016/j.braindev.2017.10.003_b0040 article-title: BAFF/APRIL system in pediatric OMS: relation to severity, neuroinflammation, and immunotherapy publication-title: J Neuroinflam doi: 10.1186/1742-2094-10-10 – volume: 156 start-page: 158 year: 2010 ident: 10.1016/j.braindev.2017.10.003_b0015 article-title: Autoimmune focal encephalitis shows marked hypermetabolism on positron emission tomography publication-title: J Pediatr doi: 10.1016/j.jpeds.2009.07.048 – volume: 162 start-page: 850 year: 2013 ident: 10.1016/j.braindev.2017.10.003_b0005 article-title: Pediatric anti-N-methyl-D-aspartate receptor encephalitis-clinical analysis and novel findings in a series of 20 patients publication-title: J Pediatr doi: 10.1016/j.jpeds.2012.10.011 – volume: 28 start-page: 417 year: 2013 ident: 10.1016/j.braindev.2017.10.003_b0050 article-title: Response to correspondence on “active comparator-controlled, rater-blinded study of corticotropin-based immunotherapies for opsoclonus-myoclonus syndrome” publication-title: J Child Neurol doi: 10.1177/0883073812469054 |
SSID | ssj0001210 |
Score | 2.1814468 |
Snippet | Immunomodulatory therapy has shown some therapeutic benefits in patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. In this report, we... |
SourceID | proquest pubmed crossref elsevier |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 247 |
SubjectTerms | ACTH therapy Anti-N-methyl-D-aspartate receptor encephalitis Autoimmune focal encephalitis Treatment |
Title | The efficacy of adrenocorticotropic hormone in a girl with anti-N-methyl-D-aspartate receptor encephalitis |
URI | https://www.clinicalkey.com/#!/content/1-s2.0-S0387760417302681 https://dx.doi.org/10.1016/j.braindev.2017.10.003 https://www.ncbi.nlm.nih.gov/pubmed/29122401 https://www.proquest.com/docview/1963271758 |
Volume | 40 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NS9xAFH_oCuKlaKt2W5Up9JrdZJLMZI7iB6ulXlrBW5hMXjSLJGFdBS_92_tePpb2IApeQhJ4JPnN5De_l_cRgO8uywz5Hdqj5SQnByVHz2jujKiNln4Wcs92zra4UrPr6PImvlmDk6EWhtMqe-7vOL1l6_7MtEdz2pTl9BcHXrXyo4AmqVRcfr0hQ6PiEWwcX_yYXa0ImXtktcEEep_Y4J9C4fkk4z8x5PjEWV560iZ6hS-tUS9p0HYtOt-GD72IFMfdfe7AGlYfYfNnHyb_BHMafIHcHMK6Z1EXwnK9dk2OJhnUy0XdlE7ckVqtKxRlJay4LRf3gr_JCkK69IhekUbw3jv1LFEOx-tREE7YkIsuGKTmjgV8-bAL1-dnv09mXv9TBc-FJlp6tsiLmDZW5SpxeaFaJ5G8ChJCOe27KMp04oxfkFTwY2k1SRprsJBBIaPChXswqujuPoNwymAgs1hpF0dodYKkRiQiGhvnmbVjmA4wpk3XOyMdksrm6QB8ysDzeQJ-DHpAOx0qQ4nLUqL3Vy3NyvK_-fMm22_DwKb0cnHExFZYPz6kTE-SHN44GcN-N-KrJ5GGg5J-8OUdV_4KW3SUdDltBzBaLh7xkETOMjuC9cmf4Kifyn8BcP38Rg |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1JS8QwFA6ioF7E3XGN4LUznXRJcxQXxvWigreQpq9OB2nLOApe_O2-18XlIApeSmn7aPolefle3xLGDmwcK7Q7pIPLSYIGSgKOklQZUSop3Nijmu0UbXEdDu788_vgfoodtbkwFFbZ6P5ap1faurnSa9DslVnWuyHHqwxdv4-DVISUfj3jB56kuL7u22ecB1XIqlwJOJvo8S9pwqNuTPswJPBCMV6yW4V5eT-tUD8x0GolOl1kCw2F5Id1K5fYFOTLbPaqcZKvsBF2PQcqDWHsKy9Sbihbu0AzEwWKybgoM8uHyFWLHHiWc8MfsvEjpz-yHHHOHFSugP336Bw7BhUOeeuBI0pQooHOCaJySPQ9e1pld6cnt0cDp9lSwbGe8ieOSZM0wIMJkzCySRpWJiLaFEiDEjy3vh_LyCo3RaLgBsJIJDRGQSr6qfBT662x6Rxbt8G4DRX0RRyE0gY-GBkBchEBAMoESWxMh_VaGHVZV87QbUjZSLfAawKeriPwHSZbtHWbF4qaTKNy_1VSfUh-Gz1_kt1vO1bj1CJ_icmheH7SpJwEmrtB1GHrdY9_fIlQ5JJ0-5v_ePMemxvcXl3qy7Priy02j3eiOrptm01Pxs-wg3RnEu9Ww_kdlyP9EQ |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=The+efficacy+of+adrenocorticotropic+hormone+in+a+girl+with+anti-N-methyl-D-aspartate+receptor+encephalitis&rft.jtitle=Brain+%26+development+%28Tokyo.+1979%29&rft.au=Hatanaka%2C+Mari&rft.au=Shimakawa%2C+Shuichi&rft.au=Okumura%2C+Akihisa&rft.au=Natsume%2C+Jun&rft.date=2018-03-01&rft.pub=Elsevier+B.V&rft.issn=0387-7604&rft.eissn=1872-7131&rft.volume=40&rft.issue=3&rft.spage=247&rft.epage=250&rft_id=info:doi/10.1016%2Fj.braindev.2017.10.003&rft.externalDocID=S0387760417302681 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0387-7604&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0387-7604&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0387-7604&client=summon |