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Year Number of Results
2004 1
2008 1
2009 1
2011 1
2012 4
2013 6
2014 6
2015 4
2016 6
2017 3
2018 4
2019 8
2020 7
2021 8
2022 11
2023 8
2024 2

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64 results

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Page 1
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.
Bachmann-Gagescu R, Dempsey JC, Phelps IG, O'Roak BJ, Knutzen DM, Rue TC, Ishak GE, Isabella CR, Gorden N, Adkins J, Boyle EA, de Lacy N, O'Day D, Alswaid A, Ramadevi A R, Lingappa L, Lourenço C, Martorell L, Garcia-Cazorla À, Ozyürek H, Haliloğlu G, Tuysuz B, Topçu M; University of Washington Center for Mendelian Genomics; Chance P, Parisi MA, Glass IA, Shendure J, Doherty D. Bachmann-Gagescu R, et al. Among authors: lingappa l. J Med Genet. 2015 Aug;52(8):514-22. doi: 10.1136/jmedgenet-2015-103087. Epub 2015 Jun 19. J Med Genet. 2015. PMID: 26092869 Free PMC article.
Diagnosis and Management of Global Development Delay: Consensus Guidelines of Growth, Development and Behavioral Pediatrics Chapter, Neurology Chapter and Neurodevelopment Pediatrics Chapter of the Indian Academy of Pediatrics.
Juneja M, Gupta A, Sairam S, Jain R, Sharma M, Thadani A, Srinivasan R, Lingappa L, Ahmed S, Multani KS, Buch P, Chatterjee N, Dalwai S, Kabra M, Kapoor S, Patel PK, Girisha KM, Kulkarni M, Kunju PAM, Malhi P, Meenai Z, Mishra D, Mundkur N, Nair MKC, Oommen SP, Prasad C, Singh A, Srivastava L, Suman P, Thakur R. Juneja M, et al. Among authors: lingappa l. Indian Pediatr. 2022 May 15;59(5):401-415. Epub 2022 Feb 19. Indian Pediatr. 2022. PMID: 35188106 Free article.
Lingappa et al. reply.
Lingappa L. Lingappa L. Dev Med Child Neurol. 2014 Jul;56(7):699-700. doi: 10.1111/dmcn.12451. Epub 2014 Apr 19. Dev Med Child Neurol. 2014. PMID: 24750040 Free article. No abstract available.
Cryptogenic posterior circulation stroke in children.
Aripirala P, Reddy N, Lingappa L, Konanki R, Varma DR, Raju S. Aripirala P, et al. Among authors: lingappa l. Dev Med Child Neurol. 2023 Jun;65(6):847-854. doi: 10.1111/dmcn.15462. Epub 2022 Nov 15. Dev Med Child Neurol. 2023. PMID: 36380707 Review.
Clinical, neuroradiological, and molecular characterization of mitochondrial threonyl-tRNA-synthetase (TARS2)-related disorder.
Accogli A, Lin SJ, Severino M, Kim SH, Huang K, Rocca C, Landsverk M, Zaki MS, Al-Maawali A, Srinivasan VM, Al-Thihli K, Schaefer GB, Davis M, Tonduti D, Doneda C, Marten LM, Mühlhausen C, Gomez M, Lamantea E, Mena R, Nizon M, Procaccio V, Begtrup A, Telegrafi A, Cui H, Schulz HL, Mohr J, Biskup S, Loos MA, Aráoz HV, Salpietro V, Keppen LD, Chitre M, Petree C, Raymond L, Vogt J, Sawyer LB, Basinger AA, Pedersen SV, Pearson TS, Grange DK, Lingappa L, McDunnah P, Horvath R, Cognè B, Isidor B, Hahn A, Gripp KW, Jafarnejad SM, Østergaard E, Prada CE, Ghezzi D, Gowda VK, Taylor RW, Sonenberg N, Houlden H, Sissler M, Varshney GK, Maroofian R. Accogli A, et al. Among authors: lingappa l. Genet Med. 2023 Nov;25(11):100938. doi: 10.1016/j.gim.2023.100938. Epub 2023 Jul 13. Genet Med. 2023. PMID: 37454282 Free article.
TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions.
Almousa H, Lewis SA, Bakhtiari S, Nordlie SH, Pagnozzi A, Magee H, Efthymiou S, Heim JA, Cornejo P, Zaki MS, Anwar N, Maqbool S, Rahman F, Neilson DE, Vemuri A, Jin SC, Yang XR, Heidari A, van Gassen K, Trimouille A, Thauvin-Robinet C, Liu J, Bruel AL, Tomoum H, Shata MO, Hashem MO, Toosi MB, Karimiani EG, Yeşil G, Lingappa L, Baruah D, Ebrahimzadeh F, Van-Gils J, Faivre L, Zamani M, Galehdari H, Sadeghian S, Shariati G, Mohammad R, van der Smagt J, Qari A, Vincent JB, Innes AM, Dursun A, Özgül RK, Akar HT, Bilguvar K, Mignot C, Keren B, Raveli C, Burglen L, Afenjar A, Kaat LD, van Slegtenhorst M, Alkuraya F, Houlden H, Padilla-Lopez S, Maroofian R, Sacher M, Kruer MC. Almousa H, et al. Among authors: lingappa l. Brain. 2024 Jan 4;147(1):311-324. doi: 10.1093/brain/awad301. Brain. 2024. PMID: 37713627
Association of Child Neurology-Indian Epilepsy Society Consensus Document on Parental Counseling of Children with Epilepsy.
Srivastava K, Sehgal R, Konanki R, Jain R, Sharma S, Mittal R; Association of Child Neurology (AOCN)-Indian Epilepsy Society (IES) SOLACE Expert Group; Hedge A, Aggarwal A, Chattopadhyay A, Patra B, Kaushik JS, Lingappa L, Sankhyan N, Kapoor P, Singhi P, Aneja S, Gulati S, Kanhere S, Rajadhyakshya S, Kalra V, Gupta VB, Udani V, Sudan Y, Mehendiratta MM, Tripathi M, Subhash GT, Bharti B, Rao S, Naseem M, Mukherjee S, Jain P, Khosla M, Shanbagh K, Jain D, Mansingh S, Yadav D, Singh C, Raina S, Srivastava S, Ahuja L, Kumar R, Vinayan KP, Jain R, Jain S, Mishra D. Srivastava K, et al. Among authors: lingappa l. Indian J Pediatr. 2019 Jul;86(7):608-616. doi: 10.1007/s12098-019-02946-z. Epub 2019 Jun 8. Indian J Pediatr. 2019. PMID: 31177510 Review.
KCTD7-related progressive myoclonic epilepsy: Report of 42 cases and review of literature.
Yoganathan S, Whitney R, Thomas M, Danda S, Chettali AM, Prasad AN, Farhan SMK, AlSowat D, Abukhaled M, Aldhalaan H, Gowda VK, Kinhal UV, Bylappa AY, Konanki R, Lingappa L, Parchuri BM, Appendino JP, Scantlebury MH, Cunningham J, Hadjinicolaou A, El Achkar CM, Kamate M, Menon RN, Jose M, Riordan G, Kannan L, Jain V, Manokaran RK, Chau V, Donner EJ, Costain G, Minassian BA, Jain P. Yoganathan S, et al. Among authors: lingappa l. Epilepsia. 2024 Mar;65(3):709-724. doi: 10.1111/epi.17880. Epub 2024 Jan 17. Epilepsia. 2024. PMID: 38231304
Case series on Silvery Hair Syndromes: Single Center Experience.
Siddiahgari S, Soma SK, Penmetcha C, Vaddadi S, Bandi V, Lingappa L. Siddiahgari S, et al. Among authors: lingappa l. Indian J Dermatol. 2022 Mar-Apr;67(2):164-168. doi: 10.4103/ijd.IJD_723_20. Indian J Dermatol. 2022. PMID: 36092238 Free PMC article.
64 results