Works matching AU Mankad, Kshitij

Results: 154
    1

    Integrating standard epilepsy protocol, ASL-perfusion, MP2RAGE/EDGE and the MELD-FCD classifier in the detection of subtle epileptogenic lesions: a 3 Tesla MRI pilot study.

    Published in:
    Neuroradiology, 2025, v. 67, n. 3, p. 665, doi. 10.1007/s00234-024-03488-8
    By:
    • Pastore, Luigi Vincenzo;
    • Sudhakar, Sniya Valsa;
    • Mankad, Kshitij;
    • De Vita, Enrico;
    • Biswas, Asthik;
    • Tisdall, Martin M.;
    • Chari, Aswin;
    • Figini, Matteo;
    • Tahir, M. Zubair;
    • Adler, Sophie;
    • Moeller, Friederike;
    • Cross, J. Helen;
    • Pujar, Suresh;
    • Wagstyl, Konrad;
    • Ripart, Mathilde;
    • Löbel, Ulrike;
    • Cirillo, Luigi;
    • D'Arco, Felice
    Publication type:
    Article
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    Tumour mimics in paediatric neuroimaging.

    Published in:
    Neuroradiology, 2025, v. 67, n. 1, p. 7, doi. 10.1007/s00234-024-03507-8
    By:
    • Coppola, Fiorenza;
    • Löbel, Ulrike;
    • Morana, Giovanni;
    • Reddy, Nihaal;
    • Mankad, Kshitij
    Publication type:
    Article
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    Approaches to supratentorial brain tumours in children.

    Published in:
    Neuroradiology, 2024, v. 66, n. 9, p. 1495, doi. 10.1007/s00234-024-03398-9
    By:
    • Sepulveda, Francisco;
    • Scotto Opipari, Raffaella;
    • Coppola, Fiorenza;
    • Ramaglia, Antonia;
    • Mankad, Kshitij;
    • Alves, Cesar A. P.;
    • Bison, Brigitte;
    • Löbel, Ulrike
    Publication type:
    Article
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    (What's the story) morning glory? MRI findings in morning glory disc anomaly.

    Published in:
    Neuroradiology, 2024, v. 66, n. 7, p. 1225, doi. 10.1007/s00234-024-03375-2
    By:
    • Ní Leidhin, Caoilfhionn;
    • Erickson, Jonathan P.;
    • Bynevelt, Michael;
    • Lam, Geoffrey;
    • Lock, Jane H.;
    • Wang, George;
    • Mankad, Kshitij;
    • Taranath, Ajay;
    • Mason, Michael;
    • Lakshmanan, Rahul;
    • Shipman, Peter;
    • Warne, Richard R.
    Publication type:
    Article
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    Pediatric nasal chondromesenchymal hamartomas: a case series.

    Published in:
    Neuroradiology, 2024, v. 66, n. 3, p. 437, doi. 10.1007/s00234-023-03276-w
    By:
    • Avsenik, Jernej;
    • Albalkhi, Ibrahem;
    • Prabhu, Sanjay P.;
    • Radhakrishnan, Rupa;
    • Goetti, Robert;
    • Jaju, Alok;
    • Merve, Ashirwad;
    • Biswas, Asthik;
    • Mankad, Kshitij
    Publication type:
    Article
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    Imaging characteristics and neurosurgical outcome in subjects with agenesis of the corpus callosum and interhemispheric cysts.

    Published in:
    Neuroradiology, 2022, v. 64, n. 11, p. 2163, doi. 10.1007/s00234-022-02990-1
    By:
    • Severino, Mariasavina;
    • Tortora, Domenico;
    • Reid, Catriona;
    • Uccella, Sara;
    • Nobili, Lino;
    • Accogli, Andrea;
    • Srour, Myriam;
    • Ramaglia, Antonia;
    • Sudhakar, Sniya;
    • Consales, Alessandro;
    • Pavanello, Marco;
    • Piatelli, Gianluca;
    • James, Greg;
    • Ravegnani, Marcello;
    • Rossi, Andrea;
    • Mankad, Kshitij
    Publication type:
    Article
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    Spinal involvement in pediatric familial cavernous malformation syndrome.

    Published in:
    Neuroradiology, 2022, v. 64, n. 8, p. 1671, doi. 10.1007/s00234-022-02958-1
    By:
    • Geraldo, Ana Filipa;
    • Luis, Aysha;
    • Alves, Cesar Augusto P. F.;
    • Tortora, Domenico;
    • Guimarães, Joana;
    • Reimão, Sofia;
    • Pavanello, Marco;
    • de Marco, Patrizia;
    • Scala, Marcello;
    • Capra, Valeria;
    • Rossi, Andrea;
    • Schwartz, Erin Simon;
    • Mankad, Kshitij;
    • Severino, Mariasavina
    Publication type:
    Article
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    Guidelines for magnetic resonance imaging in pediatric head and neck pathologies: a multicentre international consensus paper.

    Published in:
    Neuroradiology, 2022, v. 64, n. 6, p. 1081, doi. 10.1007/s00234-022-02950-9
    By:
    • D'Arco, Felice;
    • Mertiri, Livja;
    • de Graaf, Pim;
    • De Foer, Bert;
    • Popovič, Katarina S.;
    • Argyropoulou, Maria I.;
    • Mankad, Kshitij;
    • Brisse, Hervé J.;
    • Juliano, Amy;
    • Severino, Mariasavina;
    • Van Cauter, Sofie;
    • Ho, Mai-Lan;
    • Robson, Caroline D.;
    • Siddiqui, Ata;
    • Connor, Steve;
    • Bisdas, Sotirios;
    • on behalf of the Consensus for Magnetic Resonance Protocols Study (COMPS) Group;
    • Bozzao, Alessandro;
    • Sedlacik, Jan;
    • Espagnet, Camilla Rossi
    Publication type:
    Article
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    Clinical Profile and Treatment Outcomes of Hypermanganesemia with Dystonia 1 and 2 among 27 Indian Children.

    Published in:
    Movement Disorders Clinical Practice, 2022, v. 9, n. 7, p. 886, doi. 10.1002/mdc3.13516
    By:
    • Garg, Divyani;
    • Yoganathan, Sangeetha;
    • Shamim, Uzma;
    • Mankad, Kshitij;
    • Gulati, Parveen;
    • Bonifati, Vincenzo;
    • Botre, Abhijeet;
    • Kalane, Umesh;
    • Saini, Arushi Gahlot;
    • Sankhyan, Naveen;
    • Srivastava, Kavita;
    • Gowda, Vykuntaraju K.;
    • Juneja, Monica;
    • Kamate, Mahesh;
    • Padmanabha, Hansashree;
    • Panigrahi, Debasis;
    • Pachapure, Shaila;
    • Udani, Vrajesh;
    • Kumar, Atin;
    • Pandey, Sanjay
    Publication type:
    Article
    26

    Clinical features, investigations, and outcomes of pediatric limbic encephalitis: A multicenter study.

    Published in:
    Annals of Clinical & Translational Neurology, 2022, v. 9, n. 1, p. 67, doi. 10.1002/acn3.51494
    By:
    • Sabanathan, Saraswathy;
    • Abdel‐Mannan, Omar;
    • Mankad, Kshitij;
    • Siddiqui, Ata;
    • Das, Krishna;
    • Carr, Lucinda;
    • Eltze, Christin;
    • Eyre, Michael;
    • Gadian, Jon;
    • Hemingway, Cheryl;
    • Kaliakatsos, Marios;
    • Kneen, Rachel;
    • Krishnakumar, Deepa;
    • Lynch, Bryan;
    • Parida, Amitav;
    • Rossor, Thomas;
    • Taylor, Micheal;
    • Wassmer, Evangeline;
    • Wright, Sukhvir;
    • Lim, Ming
    Publication type:
    Article
    27

    L1CAM variants cause two distinct imaging phenotypes on fetal MRI.

    Published in:
    Annals of Clinical & Translational Neurology, 2021, v. 8, n. 10, p. 2004, doi. 10.1002/acn3.51448
    By:
    • Accogli, Andrea;
    • Goergen, Stacy;
    • Izzo, Giana;
    • Mankad, Kshitij;
    • Krajden Haratz, Karina;
    • Parazzini, Cecilia;
    • Fahey, Michael;
    • Menzies, Lara;
    • Baptista, Julia;
    • Carpineta, Lucia;
    • Tortora, Domenico;
    • Fulcheri, Ezio;
    • Gaetano Vellone, Valerio;
    • Paladini, Dario;
    • Spaccini, Luigina;
    • Toto, Valentina;
    • Trayers, Claire;
    • Ben Sira, Liat;
    • Reches, Adi;
    • Malinger, Gustavo
    Publication type:
    Article
    28

    Trauma musculoskeletal ultrasound.

    Published in:
    Emergency Radiology, 2008, v. 15, n. 2, p. 83, doi. 10.1007/s10140-007-0691-0
    By:
    • Kshitij Mankad;
    • Edward Hoey;
    • Andrew Grainger;
    • Dominic Barron
    Publication type:
    Article
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    A loss‐of‐function homozygous mutation in <italic>DDX59</italic> implicates a conserved DEAD‐box RNA helicase in nervous system development and function.

    Published in:
    Human Mutation, 2018, v. 39, n. 2, p. 187, doi. 10.1002/humu.23368
    By:
    • Salpietro, Vincenzo;
    • Efthymiou, Stephanie;
    • Manole, Andreea;
    • Maurya, Bhawana;
    • Wiethoff, Sarah;
    • Ashokkumar, Balasubramaniem;
    • Cutrupi, Maria Concetta;
    • Dipasquale, Valeria;
    • Manti, Sara;
    • Botia, Juan A.;
    • Ryten, Mina;
    • Vandrovcova, Jana;
    • Bello, Oscar D.;
    • Bettencourt, Conceicao;
    • Mankad, Kshitij;
    • Mukherjee, Ashim;
    • Mutsuddi, Mousumi;
    • Houlden, Henry
    Publication type:
    Article
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    Progress in the Management of Paediatric-Onset Multiple Sclerosis.

    Published in:
    Children, 2020, v. 7, n. 11, p. 1, doi. 10.3390/children7110222
    By:
    • Smith, Aphra Luchesa;
    • Benetou, Christina;
    • Bullock, Hayley;
    • Kuczynski, Adam;
    • Rudebeck, Sarah;
    • Hanson, Katie;
    • Crichton, Sarah;
    • Mankad, Kshitij;
    • Siddiqui, Ata;
    • Byrne, Susan;
    • Ming Lim;
    • Hemingway, Cheryl
    Publication type:
    Article
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    Human mutations in SLITRK3 implicated in GABAergic synapse development in mice.

    Published in:
    Frontiers in Molecular Neuroscience, 2024, p. 01, doi. 10.3389/fnmol.2024.1222935
    By:
    • Efthymiou, Stephanie;
    • Han, Wenyan;
    • Ilyas, Muhammad;
    • Jun Li;
    • Yichao Yu;
    • Scala, Marcello;
    • Malintan, Nancy T.;
    • Vavouraki, Nikoleta;
    • Mankad, Kshitij;
    • Maroofian, Reza;
    • Rocca, Clarissa;
    • Salpietro, Vincenzo;
    • Lakhani, Shenela;
    • Mallack, Eric J.;
    • Palculict, Timothy Blake;
    • Hong Li;
    • Guojun Zhang;
    • Zafar, Faisal;
    • Rana, Nuzhat;
    • Noriko Takashima
    Publication type:
    Article
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    Loss‐of‐Function Variants in HOPS Complex Genes VPS16 and VPS41 Cause Early Onset Dystonia Associated with Lysosomal Abnormalities.

    Published in:
    Annals of Neurology, 2020, v. 88, n. 5, p. 867, doi. 10.1002/ana.25879
    By:
    • Steel, Dora;
    • Zech, Michael;
    • Zhao, Chen;
    • Barwick, Katy E. S.;
    • Burke, Derek;
    • Demailly, Diane;
    • Kumar, Kishore R.;
    • Zorzi, Giovanna;
    • Nardocci, Nardo;
    • Kaiyrzhanov, Rauan;
    • Wagner, Matias;
    • Iuso, Arcangela;
    • Berutti, Riccardo;
    • Škorvánek, Matej;
    • Necpál, Ján;
    • Davis, Ryan;
    • Wiethoff, Sarah;
    • Mankad, Kshitij;
    • Sudhakar, Sniya;
    • Ferrini, Arianna
    Publication type:
    Article
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