부산대학교 도서관

Šikić, K.; Petković Ramadža, D.; Žigman, T.; Davidović, M.; Huljev Frković, S.; Barić, I.; Peters, T.M.A.; Engelke, U.; Wevers, R.A.; Fumić, K.; Körmendy, T.; Martinelli, D.; Novelli, A.; Lepri, F.R.

(JIMD Reports, November 2024, 65(6):361-370)

Kirk, F.T.; Munk, D.E.; Vilstrup, H.; Ott, P.; Damgaard Sandahl, T.; Ek, J.; Birk Møller, L.; Bendixen Thorup, M.; Hvid Danielsen, E.

In: Frontiers in Neurology. (Frontiers in Neurology, 1 September 2022, 13)

Chiplunkar, S.; Bindu, P.S.; Nagappa, M.; Govindaraj, P.; Gayathri, N.; Bharath, M.M.S.; Taly, A.B.; Bineesh, C.; Mathuranath, P.S.; Sinha, S.; Arvinda, H.R.

In: Metabolic Brain Disease. (Metabolic Brain Disease, 1 October 2016, 31(5):1195-1198)

Hirn, Emma; Huppke, Brenda; Wilken, Bernd; Kiehntopf, Michael; Huppke, Peter

PEDIATRIC NEUROLOGY; NOV 2025, 172 p1-p7, 7p.

Wong, Keit Men; Maroofian, Reza; Meier, Kolja; Diegmann, Susann; Tkemaladze, Tinatin; Alvi, Javeria Raza; Tasharrofi, Behnoosh; Efthymiou, Stephanie; Munchau, Alexander; Korenke, G. Christoph; Almontashiri, Naif; Eyaid, Wafaa; Kashgari, Amna; Alotaibi, Modhi; Gaertner, Jutta; Huppke, Brenda; Asadollahi, Mostafa; Chikvinidze, Gocha; Keramatipour, Mohammad; Sultan, Tipu; Thiele, Holger; Nuernberg, Peter; Graeler, Markus H.; Houlden, Henry; Huppke, Peter

MOVEMENT DISORDERS; JUL 1 2025, 15p.

Lindemann M; Department of Neurosurgery, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Januzi D; Department of Neurosurgery, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Borowski S; Department of Pediatric Neurology, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Neumeister A; Department of Neurosurgery, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Löschner D; Department of Neurosurgery, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Dubinski D; Department of Neurosurgery, University Medicine Rostock, Rostock, Germany.; Huppke P; Department of Pediatric Neurology, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Senft C; Department of Neurosurgery, University Hospital Jena, Friedrich Schiller University, Jena, Germany.; Baumgarten P; Department of Neurosurgery, University Hospital Jena, Friedrich Schiller University, Jena, Germany.

Publisher: Elsevier B.V Country of Publication: Netherlands NLM ID: 9918470888906676 Publication Model: eCollection Cited Medium: Internet ISSN: 2772-5294 (Electronic) Linking ISSN: 27725294 NLM ISO Abbreviation: Brain Spine Subsets: PubMed not MEDLINE

Huppke, Liam; Gebhardt, Christina; Grumme, Lea; Lichtnekert, Julia; Singh, Delila; Ullrich, Fabian T. H.; Wolfrum, Stefan; Skapenko, Alla; Schulze-Koops, Hendrik

RHEUMATOLOGY INTERNATIONAL; OCT 23 2025, 45 11, p254 8p.

Storm van's Gravesande, K.; Calabrese, P.; Blaschek, A.; Rostásy, K.; Huppke, P.; Rothe, L.; Mall, V.; Kessler, J.; Kalbe, E.; Kraus, V.; Dornfeld, E.; Elpers, C.; Lohmann, H.; Weddige, A.; Hagspiel, S.; Kirschner, J.; Brehm, M.; Blank, C.; Schubert, J.; Schimmel, M.; Pacheè, S.; Mohrbach, M.; Karenfort, M.; Kamp, G.; Lücke, T.; Neumann, H.; Lutz, Sabine; Gierse, A.; Sievers, S.; Schiffmann, H.; de Soye, I.; Trollmann, R.; Candova, A.; Rosner, M.; Neu, A.; Romer, G.; Seidel, U.; John, R.; Hofmann, C.; Schulz; Kinder, S.; Bertolatus, A.; Scheidtmann, K.; Lasogga, R.; Leiz, S.; Alber, M.; Kranz, J.; Bajer-Kornek, B.; Seidl, R.; Novak, A.; Storm van’s Gravesande, K.

European Journal of Paediatric Neurology. 23:792-800

Huppke, Brenda; de Vries, Heike; Blaschek, Astrid; Huppke, Peter

NEUROPEDIATRICS; DEC 20 2024, 4p.

Huppke, Peter; Gartner, Jutta

MONATSSCHRIFT KINDERHEILKUNDE; NOV 18 2025, 3p.

Held, Friederike; Bayas, Antonios; Berthele, Achim; Christe, Katharina; Dettmers, Christian; Domurath, Burkhard; Ebert, Juliane; Fasshauer, Edeltraut; Flachenecker, Peter; Gaertner, Jutta; Hasanbasic, Dzenita; Heesen, Christoph; Hegen, Harald; Thomas, Henze; Huppke, Peter; Khalil, Michael; Kirschner-Hermanns, Ruth; Korn, Thomas; Kuempfel, Tania; Lamprecht, Sabine; Luessi, Felix; Meier, Uwe; Hoerste, Gerd Meyerzu; Maeurer, Mathias; Oertel, Frederike Cosima; Pot, Caroline; Proebstel, Anne-Katrin; Rostasy, Kevin; Salmen, Anke; Scheiderbauer, Jutta; Schmidt, Markus; Stark, Erwin; Trebst, Corinna; Trollmann, Regina; Warnke, Clemens; Wattjes, Mike P.; Benedikt, Wiestler; Wildemann, Brigitte; Zimmermann, Uwe; Gehring, Klaus; Hemmer, Bernhard

MULTIPLE SCLEROSIS JOURNAL; SEP 2025, 31 3, p138-p140, 3p. Supplement: S

Whittam, D H; Karthikeayan, V; Gibbons, E; Kneen, R; Chandratre, S; Ciccarelli, O; Hacohen, Y; de Seze, J; Deiva, K; Hintzen, R Q; Wildemann, B; Jarius, S; Kleiter, I; Rostasy, K; Huppke, P; Hemmer, B; Paul, F; Aktas, O; Pröbstel, A K; Arrambide, G; Tintore, M; Amato, M P; Nosadini, M; Mancardi, M M; Capobianco, M; Illes, Z; Siva, A; Altintas, A; Akman-Demir, G; Pandit, L; Apiwattankul, M; Hor, J Y; Viswanathan, S; Qiu, W; Kim, H J; Nakashima, I; Fujihara, K; Ramanathan, S; Dale, R C; Boggild, M; Broadley, S; Lana-Peixoto, M A; Sato, D K; Tenembaum, S; Cabre, P; Wingerchuk, D M; Weinshenker, B G; Greenberg, B; Matiello, M; Klawiter, E C; Bennett, J L; Wallach, A I; Kister, I; Banwell, B L; Traboulsee, A; Pohl, D; Palace, J; Leite, M I; Levy, M; Marignier, R; Solomon, T; Lim, M; Huda, S; Jacob, A

Whittam, D H, Karthikeayan, V, Gibbons, E, Kneen, R, Chandratre, S, Ciccarelli, O, Hacohen, Y, de Seze, J, Deiva, K, Hintzen, R Q, Wildemann, B, Jarius, S, Kleiter, I, Rostasy, K, Huppke, P, Hemmer, B, Paul, F, Aktas, O, Pröbstel, A K, Arrambide, G, Tintore, M, Amato, M P, Nosadini, M, Mancardi, M M, Capobianco, M, Illes, Z, Siva, A, Altintas, A, Akman-Demir, G, Pandit, L, Apiwattankul, M, Hor, J Y, Viswanathan, S, Qiu, W, Kim, H J, Nakashima, I, Fujihara, K, Ramanathan, S, Dale, R C, Boggild, M, Broadley, S, Lana-Peixoto, M A, Sato, D K, Tenembaum, S, Cabre, P, Wingerchuk, D M, Weinshenker, B G, Greenberg, B, Matiello, M, Klawiter, E C, Bennett, J L, Wallach, A I, Kister, I, Banwell, B L, Traboulsee, A, Pohl, D, Palace, J, Leite, M I, Levy, M, Marignier, R, Solomon, T, Lim, M, Huda, S & Jacob, A 2020, ' Treatment of MOG antibody associated disorders : results of an international survey ', Journal of Neurology, vol. 267, no. 12, pp. 3565–3577 . https://doi.org/10.1007/s00415-020-10026-y

Hummel-Abmeier, Hannah; Naxer, Sabine; Kadas, Ella Maria; Zimmermann, Hanna; Knaack, Bianca; Huppke, Peter; Kowallick, Antonia; Meier, Kolja; Brandt, Alexander Ulrich; Paul, Friedemann; Schittkowski, Michael; Oertel, Frederike Cosima; Gaertner, Jutta

NEUROLOGY-NEUROIMMUNOLOGY & NEUROINFLAMMATION; MAY 2025, 12 3, pe200387 10p.

L. Peña‐Quintana; G. Scherer; M.L. Curbelo‐Estévez; F. Jiménez‐Acosta; B. Hartmann; F. La Roche; S. Meavilla‐Olivas; C. Pérez‐Cerdá; N. García‐Segarra; Y. Giguère; P. Huppke; G.A. Mitchell; E. Mönch; D. Trump; C. Vianey‐Saban; E.R. Trimble; I. Vitoria‐Miñana; D. Reyes‐Suárez; T. Ramírez‐Lorenzo; A. Tugores

CLINICAL GENETICS
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Clinical Genetics [ISSN 0009-9163], v. 92 (3), p. 306-317
accedaCRIS portal de investigación de la Universidad de las Palmas de Gran Canaria
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Instituto de Investigación Sanitaria La Fe (IIS La Fe)

Whittam, D. H.; Chandratre, S.; Ciccarelli, O.; de Seze, J.; Deiva, K.; Hintzen, R. Q.; Wildemann, B.; Jarius, S.; Kleiter, I.; Rostasy, K.; Huppke, P.; Hemmer, B.; Paul, F.; Probstel, A. K.; Tintore, M.; Amato, M. P.; Nosadini, M.; Mancardi, M. M.; Capobianco, M.; Illes, Z.; Siva, A.; Altintas, A.; Akman-Demir, G.; Pandit, L.; Apiwattankul, M.; Hor, J. Y.; Viswanathan, S.; Qiu, W.; Fujihara, K.; Ramanathan, S.; Dale, R. C.; Boggild, M.; Broadley, S.; Lana-Peixoto, M. A.; Tenembaum, S.; Cabre, P.; Wingerchuk, D. M.; Greenberg, B.; Weinshenker, B. G.; Klawiter, E. C.; Bennett, J. L.; Wallach, A. I.; Kister, I.; Banwell, B. L.; Traboulsee, A.; Pohl, D.; Palace, J.; Leite, M. I.; Marignier, R.; Jacob, A.

Whittam, D H, Chandratre, S, Ciccarelli, O, de Seze, J, Deiva, K, Hintzen, R Q, Wildemann, B, Jarius, S, Kleiter, I, Rostasy, K, Huppke, P, Hemmer, B, Paul, F, Probstel, A K, Tintore, M, Amato, M P, Nosadini, M, Mancardi, M M, Capobianco, M, Illes, Z, Siva, A, Altintas, A, Akman-Demir, G, Pandit, L, Apiwattankul, M, Hor, J Y, Viswanathan, S, Qiu, W, Fujihara, K, Ramanathan, S, Dale, R C, Boggild, M, Broadley, S, Lana-Peixoto, M A, Tenembaum, S, Cabre, P, Wingerchuk, D M, Greenberg, B, Weinshenker, B G, Klawiter, E C, Bennett, J L, Wallach, A I, Kister, I, Banwell, B L, Traboulsee, A, Pohl, D, Palace, J, Leite, M I, Marignier, R & Jacob, A 2019, ' Treatment of MOG antibody associated disorders: results of an international survey ', Multiple Sclerosis Journal, vol. 25, no. 2 Suppl. 1, P735, pp. 369-371 . https://doi.org/10.1177/1352458519868080

Bertrand M; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Shah G; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Pedersen BS; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.; Schulz A; Institute of Human Genetics, Jena University Hospital, Jena, Germany.; Weise A; Institute of Human Genetics, Jena University Hospital, Jena, Germany.; Center for Rare Diseases, Jena University Hospital, Jena, Germany.; Liehr T; Institute of Human Genetics, Jena University Hospital, Jena, Germany.; Center for Rare Diseases, Jena University Hospital, Jena, Germany.; Huppke P; Center for Rare Diseases, Jena University Hospital, Jena, Germany.; Department of Neuropediatrics, Jena University Hospital, Jena, Germany.; DiTroia S; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Quinlan AR; Department of Human Genetics, University of Utah, Salt Lake City, UT, USA.; Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT, USA.; Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tuebingen, Tuebingen, Germany.; Husain RA; Center for Rare Diseases, Jena University Hospital, Jena, Germany.; Department of Neuropediatrics, Jena University Hospital, Jena, Germany.

Publisher: S. Karger Country of Publication: Switzerland NLM ID: 101525192 Publication Model: Print-Electronic Cited Medium: Print ISSN: 1661-8769 (Print) Linking ISSN: 16618769 NLM ISO Abbreviation: Mol Syndromol Subsets: PubMed not MEDLINE

Husain RA; Department of Neuropediatrics, Jena University Hospital, 07747 Jena, Germany.; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany.; Jiao X; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.; Hennings JC; Institute of Human Genetics, Jena University Hospital, 07747 Jena, Germany.; Giesecke J; Department of Anaesthesiology and Intensive Care Medicine, Jena University Hospital, Member of the Leibniz Center for Photonics in Infection Research (LPI), 07747 Jena, Germany.; Palsule G; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.; Beck-Wödl S; Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany.; Osmanović D; Institute of Human Genetics, Jena University Hospital, 07747 Jena, Germany.; Bjørgo K; Department of Medical Genetics, Oslo University Hospital, 0424 Oslo, Norway.; Mir A; Department of Biological Sciences, Faculty of Sciences, International Islamic University, Islamabad 44000, Pakistan.; Ilyas M; Department of Biological Sciences, Faculty of Sciences, International Islamic University, Islamabad 44000, Pakistan.; Abbasi SM; Department of Biological Sciences, Faculty of Sciences, International Islamic University, Islamabad 44000, Pakistan.; Efthymiou S; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Dominik N; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Maroofian R; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Houlden H; Department of Neuromuscular Disorders, UCL Queen Square Institute of Neurology, London, WC1N 3BG, UK.; Rankin J; Department of Clinical Genetics, Royal Devon University Hospital, Exeter, EX1 2ED, UK.; Pagnamenta AT; Oxford NIHR Biomedical Research Centre, Wellcome Centre for Human Genetics, Oxford, OX3 7BN, UK.; Nashabat M; Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; Altwaijri W; Department of Pediatrics, Neurology Division, King Abdullah Specialist Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; Alfadhel M; Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; Genetics and Precision Medicine Department, King Abdullah Specialized Children's Hospital, King Abdulaziz Medical City, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; Umair M; Medical Genomics Research Department, King Abdullah International Medical Research Center, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; King Saud Bin Abdulaziz University for Health Sciences, Ministry of National Guard Health Affairs, Riyadh 11426, Saudi Arabia.; Khouj E; Department of Translational Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.; Reardon W; Blackrock Clinic, Dublin, A94 E4X7, Ireland.; El-Hattab AW; Department of Clinical Sciences, College of Medicine, University of Sharjah, 27272, Sharjah, United Arab Emirates.; Department of Pediatrics, University Hospital Sharjah, 72772, Sharjah, United Arab Emirates.; Mekki M; Department of Pediatrics, University Hospital Sharjah, 72772, Sharjah, United Arab Emirates.; Houge G; Department of Medical Genetics, Haukeland University Hospital, 5021 Bergen, Norway.; Beetz C; Centogene GmbH, 18055 Rostock, Germany.; Bauer P; Centogene GmbH, 18055 Rostock, Germany.; Putoux A; Groupement Hospitalier Est, Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, 69677 Bron Cedex, France.; Équipe GENDEV, Centre de Recherche en Neurosciences de Lyon, Univ Lyon, Univ Lyon 1, INSERM U1028 CNRS UMR5292, 69008 Lyon, France.; Lesca G; Groupement Hospitalier Est, Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, 69677 Bron Cedex, France.; Physiopathologie et Génétique du Neurone et du Muscle, Univ Lyon, Univ Lyon 1, CNRS, INSERM, UMR5261, U1315, Institut NeuroMyoGène, 69008 Lyon, France.; Sanlaville D; Groupement Hospitalier Est, Hospices Civils de Lyon, Service de Génétique, Centre de Référence Anomalies du Développement, 69677 Bron Cedex, France.; Physiopathologie et Génétique du Neurone et du Muscle, Univ Lyon, Univ Lyon 1, CNRS, INSERM, UMR5261, U1315, Institut NeuroMyoGène, 69008 Lyon, France.; Alkuraya FS; Department of Translational Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh 11211, Saudi Arabia.; Taylor RW; Wellcome Centre for Mitochondrial Research, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, NE2 4HH, UK.; NHS Highly Specialised Service for Rare Mitochondrial Disorders, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, NE1 4LP, UK.; Mentzel HJ; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany.; Section of Pediatric Radiology, Department of Radiology, Jena University Hospital, 07747 Jena, Germany.; Hübner CA; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany.; Institute of Human Genetics, Jena University Hospital, 07747 Jena, Germany.; Huppke P; Department of Neuropediatrics, Jena University Hospital, 07747 Jena, Germany.; Center for Rare Diseases, Jena University Hospital, 07747 Jena, Germany.; Hart RP; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.; Haack TB; Institute of Medical Genetics and Applied Genomics, University of Tübingen, 72076 Tübingen, Germany.; Kiledjian M; Department of Cell Biology and Neuroscience, Rutgers University, Piscataway, NJ 08854, USA.; Rubio I; Department of Anaesthesiology and Intensive Care Medicine, Jena University Hospital, Member of the Leibniz Center for Photonics in Infection Research (LPI), 07747 Jena, Germany.; Center for Sepsis Control and Care, Jena University Hospital, 07747 Jena, Germany.

Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Hummel-Abmeier H; Naxer S; Kadas EM; Zimmermann H; Knaack B; Huppke P; Kowallick A; Meier K; Brandt AU; Paul F; Schittkowski M; Oertel FC; Gärtner J

Publisher: Wolters Kluwer Health/Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 101636388 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2332-7812 (Electronic) Linking ISSN: 23327812 NLM ISO Abbreviation: Neurol Neuroimmunol Neuroinflamm Subsets: MEDLINE; PubMed not MEDLINE

Reinert, Marie-Christine; Huppke, Brenda; Hummel-Abmeier, Hannah; Stark, Wiebke; Gaertner, Jutta; Huppke, Peter

NEUROLOGY; NOV 7 2023, 101 19, pE1873-pE1883, 11p.

Wong, Keit Men; Wegener, Eike; Baradaran-Heravi, Alireza; Huppke, Brenda; Gaertner, Jutta; Huppke, Peter

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES; JUL 2023, 24 14, p11665 17p.