Works matching Congenital muscular dystrophy

Results: 861

Kongenitální svalové dystrofie.

Published in:

Neurologie Pro Praxi, 2022, v. 23, n. 1, p. 18

By:

Havlín, Ondřej;
Bálintová, Zdenka;
Juříková, Lenka;
Ošlejšková, Hana

Publication type:

Article

A Mosaic Mutation in the LAMA2 Gene in a Case of Merosin-deficient Congenital Muscular Dystrophy.

Published in:

Frontiers in Genetics, 2021, v. 12, p. 1, doi. 10.3389/fgene.2021.686800

By:

Chausova, P. A.;
Ryzhkova, O. P.;
Rudenskaya, G. E.;
Chernykh, V. B.;
Shchagina, O. A.;
Polyakov, A. V.

Publication type:

Article

Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients.

Published in:

Frontiers in Genetics, 2023, p. 1, doi. 10.3389/fgene.2023.1183663

By:

Van Khanh Tran;
Ngoc-Lan Nguyen;
Lan Ngoc Thi Tran;
Phuong Thi Le;
Anh Hai Tran;
Pham, Tuan L. A.;
Nguyen Thi Kim Lien;
Nguyen Thi Xuan;
Le Tat Thanh;
Thanh Van Ta;
Thinh Huy Tran;
Huy-Hoang Nguyen

Publication type:

Article

New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families.

Published in:

Neurogenetics, 2004, v. 5, n. 1, p. 27, doi. 10.1007/s10048-003-0165-9

By:

Louhichi, Nacim;
Triki, Chahnez;
Quijano-Roy, Susana;
Richard, Pascale;
Makri, Samira;
Méziou, Mériem;
Estournet, Brigitte;
Mrad, Slah;
Romero, Norma B.;
Ayadi, Hammadi;
Guicheney, Pascale;
Fakhfakh, Faiza

Publication type:

Article

Konjenital Musküler Distrofi Tanılı Bir Hastanın Palyatif Bakımında Henderson Hemşirelik Modeli’nin Uygulanması: Olgu Sunumu.

Published in:

Gümüshane Üniversitesi Saglik Bilimleri Dergisi, 2025, v. 14, n. 1, p. 429, doi. 10.37989/gumussagbil.1369122

By:

İLHAN, Hatice

Publication type:

Article

Autophagy increase in Merosin-Deficient Congenital Muscular Dystrophy type 1A.

Published in:

European Journal of Translational Myology, 2023, v. 33, n. 3, p. 1, doi. 10.4081/ejtm.2023.11501

By:

Mastrapasqua, Mariangela;
Rossi, Roberta;
De Cosmo, Lucrezia;
Resta, Annalisa;
Errede, Mariella;
Bizzoca, Antonella;
Zampatti, Stefania;
Resta, Nicoletta;
Giardina, Emiliano;
Ruggieri, Maddalena;
Virgintino, Daniela;
Annese, Tiziana;
Laforgia, Nicola;
Girolamo, Francesco

Publication type:

Article

Merosin-Deficient Congenital Muscular Dystrophy with Polymicrogyria and Subcortical Heterotopia: A Case Report.

Published in:

Neonatal Medicine, 2016, v. 23, n. 3, p. 173, doi. 10.5385/nm.2016.23.3.173

By:

Young Mi Han;
Na Rae Lee;
Mi Hye Bae;
Kyung Hee Park;
Jin Hong Shin;
Dae Seong Kim;
Shin Yun Byun

Publication type:

Article

Congenital muscular dystrophy-associated inflammatory chemokines provide axes for effective recruitment of therapeutic adult stem cell into muscles.

Published in:

Stem Cell Research & Therapy, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13287-020-01979-y

By:

Alexeev, Vitali;
Olavarria, Jacquelyn;
Bonaldo, Paolo;
Merlini, Luciano;
Igoucheva, Olga

Publication type:

Article

Is the Next Generation Sequencing the Essential Tool for the Early Diagnostic Approach in Congenital Muscular Dystrophy? New Mutation in the Gen LMNA Associated with Serious Phenotype.

Published in:

2021

By:

Avila, Guillermo;
González, Ana;
Abad, Araceli;
Fournier, Belén;
León, Soraya;
Corral, Jaime;
Fernández, Carlos;
Avila, Guillermo Martin;
González, Ana Pinel;
Fournier, Belén Gil;
León, Soraya Ramiro;
Corral, Jaime Antonio Medranda;
Fernández, Carlos Piquero

Publication type:

Case Study

Merosin-deficient congenital muscular dystrophy type 1A: A case report.

Published in:

2013

By:

ZHANWEN HE;
XIANGYANG LUO;
LIYANG LIANG;
PINGGAN LI;
DONGFANG LI;
MENG ZHE

Publication type:

Case Study

Megaconial congenital muscular dystrophy due to novel CHKB variants: a case report and literature review.

Published in:

Skeletal Muscle, 2022, v. 12, n. 1, p. 1, doi. 10.1186/s13395-022-00306-8

By:

Magri, Francesca;
Antognozzi, Sara;
Ripolone, Michela;
Zanotti, Simona;
Napoli, Laura;
Ciscato, Patrizia;
Velardo, Daniele;
Scuvera, Giulietta;
Nicotra, Valeria;
Giacobbe, Antonella;
Milani, Donatella;
Fortunato, Francesco;
Garbellini, Manuela;
Sciacco, Monica;
Corti, Stefania;
Comi, Giacomo Pietro;
Ronchi, Dario

Publication type:

Article

Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care.

Published in:

2017

By:

Heller, Felice;
Dabaj, Ivana;
Mah, Jean K.;
Bergounioux, Jean;
Essid, Aben;
Bönnemann, Carsten G.;
Rutkowski, Anne;
Bonne, Gisèle;
Quijano-Roy, Susana;
Wahbi, Karim;
Bönnemann, Carsten G

Publication type:

journal article

Konjenital musküler distrofili hastalarımızın değerlendirilmesi.

Published in:

Türk Pediatri Arşivi, 2009, v. 44, n. 1, p. 23

By:

Yiş, Uluç;
Uyanık, Gökhan;
Kurul, Semra Hız;
×akmakçı, Handan;
Özer, Erdener;
Dirik, Eray;
Hehr, Ute;
Morris-Rosendahl, Deborah J.

Publication type:

Article

Mutations in LAMA2 and CAPN3 genes associated with genetic and phenotypic heterogeneities within a single consanguineous family involving both congenital and progressive muscular dystrophies.

Published in:

Bioscience Reports, 2011, v. 31, n. 2, p. 125, doi. 10.1042/BSR20100026

By:

SALEM, Ikhlass HADJ;
KAMOUN, Fatma;
LOUHICHI, Nacim;
ROUIS, Souad;
MZIOU, Mariam;
FENDRI-KRIAA, Nourhene;
MAKNI-AYADI, Fatma;
TRIKI, Chahnez;
FAKHFAKH, Faiza

Publication type:

Article

A novel variant in the COL6A1 gene causing Ullrich congenital muscular dystrophy in a consanguineous family: a case report.

Published in:

2021

By:

Sirisena, Nirmala Dushyanthi;
Samaranayake, U. M. Jayami Eshana;
Neto, Osorio Lopes Abath;
Foley, A. Reghan;
Pathirana, B. A. P. Sajeewani;
Neththikumara, Nilaksha;
Paththinige, C. Sampath;
Rathnayake, Pyara;
Donkervoort, Sandra;
Bönnemann, Carsten G.;
Dissanayake, Vajira H. W.

Publication type:

journal article

Systemic inhibition of bone morphogenetic protein 1.3 as a possible treatment for laminin-related congenital muscular dystrophy.

Published in:

International Orthopaedics, 2025, v. 49, n. 1, p. 45, doi. 10.1007/s00264-024-06389-w

By:

Matic Jelic, Ivona;
Stokovic, Nikola;
Ivanjko, Natalia;
Pecina, Marko;
Kufner, Vera;
Bordukalo Niksic, Tatjana;
Vukicevic, Slobodan

Publication type:

Article

Novel synonymous substitution in POMGNT1 promotes exon skipping in a patient with congenital muscular dystrophy.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 6, p. 565, doi. 10.1007/s10038-008-0263-5

By:

Oliveira, Jorge;
Soares-Silva, Isabel;
Fokkema, Ivo;
Gonçalves, Ana;
Cabral, Alexandra;
Diogo, Luísa;
Galán, Lucía;
Guimarães, António;
Fineza, Isabel;
Dunnen, Johan;
Santos, Rosário

Publication type:

Article

CNS findings in congenital muscular dystrophy 1A (with laminin alpha-2-deficiency).

Published in:

Translational Neuroscience, 2011, v. 2, n. 2, p. 138, doi. 10.2478/s13380-011-0020-7

By:

Köhler, Cornelia;
Weigt-Usinger, Katharina;
Heyer, Christoph;
Thiels, Charlotte;
Dekomien, Gabriele;
Vorgerd, Matthias;
Lücke, Thomas

Publication type:

Article

A new congenital muscular dystrophy with mitochondrial structural abnormalities.

Published in:

1998

By:

Nishino, Ichizo;
Kobayashi, Osamu;
Goto, Yu-ichi;
Kurihara, Mana;
Kumagai, Komei;
Fujita, Takehisa;
Hashimoto, Kiyoshi;
Horai, Satoshi;
Nonaka, Ikuya;
Nishino, I;
Kobayashi, O;
Goto, Y;
Kurihara, M;
Kumagai, K;
Fujita, T;
Hashimoto, K;
Horai, S;
Nonaka, I

Publication type:

journal article

A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family.

Published in:

2024

By:

Maiga, Alassane Baneye;
Pamanta, Ibrahim;
Bamba, Salia;
Cissé, Lassana;
Diarra, Salimata;
Touré, Sidi;
Yalcouyé, Abdoulaye;
Diallo, Seydou;
Diallo, Salimata;
Kané, Fousseyni;
Diallo, Seybou Hassane;
Ba, Hamidou Oumar;
Guinto, Cheick Oumar;
Fischbeck, Kenneth;
Landoure, Guida;
Cissé, Idrissa Ahmadou

Publication type:

Case Study

Novel mutation identification and copy number variant detection via exome sequencing in congenital muscular dystrophy.

Published in:

Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 11, p. 1, doi. 10.1002/mgg3.1387

By:

Cauley, Edmund S.;
Pittman, Alan;
Mummidivarpu, Swati;
Karimiani, Ehsan G.;
Martinez, Samantha;
Moroni, Isabella;
Boostani, Reza;
Podini, Daniele;
Mora, Marina;
Jamshidi, Yalda;
Hoffman, Eric P.;
Manzini, M. Chiara

Publication type:

Article

Coexistence of Megaconial Congenital Muscular Dystrophy and Cystinuria: Mimicking Hypotonia-Cystinuria Syndrome.

Published in:

Molecular Syndromology, 2022, v. 13, n. 3, p. 240, doi. 10.1159/000520502

By:

Surucu Kara, Ilknur;
Oncul, Ummuhan;
Kose, Engin;
Turan, Husnu Mutlu;
Ceylan, Ahmet Cevdet;
Eminoglu, Fatma Tuba

Publication type:

Article

Ullrich Congenital Muscular Dystrophy.

Published in:

Iranian Journal of Child Neurology, 2011, v. 5, n. 3, p. 1

By:

HALILOGLU, Goknur;
TOPALOGLU, Haluk

Publication type:

Article

Identification of a novel LAMA2 c.2217G > A, p.(Trp739*) mutation in a Moroccan patient with congenital muscular dystrophy: a case report.

Published in:

BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-00959-2

By:

El Kadiri, Youssef;
Ratbi, Ilham;
Laarabi, Fatima Zahra;
Kriouile, Yamna;
Sefiani, Abdelaziz;
Lyahyai, Jaber

Publication type:

Article

Rhabdomyolysis Associated With Human Parvovirus B19 Infection in a Patient With Fukuyama-Type Congenital Muscular Dystrophy.

Published in:

Journal of Child Neurology, 2014, v. 29, n. 7, p. 977, doi. 10.1177/0883073813485132

By:

Ishikawa, Aki;
Yoto, Yuko;
Ohya, Kazuhiro;
Tsugawa, Takeshi;
Tsutsumi, Hiroyuki

Publication type:

Article

Peripheral Nerve Involvement in Fukuyama Congenital Muscular Dystrophy: A Case Report.

Published in:

2013

By:

Jang, Dae-Hyun;
Sung, In Young;
Ko, Tae Sung

Publication type:

Case Study

Consensus Statement on Standard of Care for Congenital Muscular Dystrophies.

Published in:

Journal of Child Neurology, 2010, v. 25, n. 12, p. 1559, doi. 10.1177/0883073810381924

By:

Wang, Ching H.;
Bonnemann, Carsten G.;
Rutkowski, Anne;
Sejersen, Thomas;
Bellini, Jonathan;
Battista, Vanessa;
Florence, Julaine M.;
Schara, Ulrike;
Schuler, Pamela M.;
Wahbi, Karim;
Aloysius, Annie;
Bash, Robert O.;
Béroud, Christophe;
Bertini, Enrico;
Bushby, Kate;
Cohn, Ronald D.;
Connolly, Anne M.;
Deconinck, Nicolas;
Desguerre, Isabelle;
Eagle, Michelle

Publication type:

Article

Вродена мускулна дистрофия с тежко засягане на централната нервна система при пациент с хомозиготна мутация в ген POMGNT1.

Published in:

Pediatria, 2022, v. 62, n. 3, p. 29

By:

Родопска, Е.;
Божинова, В.;
Топалов, Н.;
Александрова, И.;
Асенова, А.;
Шокова, А.;
Въжарова, Р.

Publication type:

Article

Cross-Sectional Study of the Association Between Plasma Brain Natriuretic Peptide Levels and Left Ventricular Shortening Fraction in Fukuyama Congenital Muscular Dystrophy.

Published in:

Tohoku Journal of Experimental Medicine, 2025, v. 266, n. 1, p. 81, doi. 10.1620/tjem.2024.J137

By:

Takatoshi Sato;
Yuki Kihara;
Kumiko Ishiguro;
Minobu Shichiji;
Terumi Murakami;
Satoru Nagata;
Eriko Shimada;
Kei Inai;
Atsuhito Takeda;
Keiko Ishigaki

Publication type:

Article

Motor Outcome Measures in Pediatric Patients with Congenital Muscular Dystrophies: A Scoping Review.

Published in:

Applied Sciences (2076-3417), 2023, v. 13, n. 2, p. 1204, doi. 10.3390/app13021204

By:

Cavallina, Ilaria;
D'Alessandro, Rossella;
Brusa, Chiara;
Panero, Elisa;
Rolle, Enrica;
Rossi, Francesca;
Mongini, Tiziana;
Ricci, Federica Silvia

Publication type:

Article

The cerebellar and thalamic degeneration in Fukuyama-type congenital muscular dystrophy.

Published in:

Acta Neuropathologica, 2000, v. 99, n. 2, p. 209, doi. 10.1007/PL00007426

By:

Kumada, Satoko;
Tsuchiya, Kuniaki;
Takahashi, Mafuyu;
Takesue, Masaro;
Shiotsu, Hidetoshi;
Nomura, Yoshiko;
Segawa, Masaya;
Ikeda, Kenji;
Hayashi, Masaharu

Publication type:

Article

Small size of orthogonal array in muscle plasma membrane of Fukuyama type congenital muscular dystrophy.

Published in:

Acta Neuropathologica, 1986, v. 72, n. 2, p. 130, doi. 10.1007/BF00685974

By:

Wakayama, Y.;
Kumagai, T.;
Jimi, T.

Publication type:

Article

Úskalí dia gnostiky atypické formy kongenitální svalové dystrofie - parciálního defi citu merosinu - kazuistiky.

Published in:

Česká a Slovenská Neurologie a Neurochirurgie, 2017, v. 80, n. 1, p. 101, doi. 10.14735/amcsnn2017101

By:

Slabá, A.;
Fajkusová, L.;
Stehlíková, K.;
Barresi, R.;
Kynčl, M.;
Zámečník, J.;
Haberlová, J.

Publication type:

Article

Brain Dysfunction in LAMA2-Related Congenital Muscular Dystrophy: Lessons From Human Case Reports and Mouse Models.

Published in:

Frontiers in Molecular Neuroscience, 2020, v. 13, p. 1, doi. 10.3389/fnmol.2020.00118

By:

Arreguin, Andrea J.;
Colognato, Holly

Publication type:

Article

ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.

Published in:

Brain: A Journal of Neurology, 2013, v. 136, n. 1, p. 269

By:

Cirak, Sebahattin;
Foley, Aileen Reghan;
Herrmann, Ralf;
Willer, Tobias;
Yau, Shu;
Stevens, Elizabeth;
Torelli, Silvia;
Brodd, Lina;
Kamynina, Alisa;
Vondracek, Petr;
Roper, Helen;
Longman, Cheryl;
Korinthenberg, Rudolf;
Marrosu, Gianni;
Nürnberg, Peter;
Michele, Daniel E.;
Plagnol, Vincent;
Hurles, Matt;
Moore, Steven A.;
Sewry, Caroline A.

Publication type:

Article

Hemodynamic instability during prone spine surgery in a patient with merosin-deficient congenital muscular dystrophy.

Published in:

Pediatric Anesthesia, 2013, v. 23, n. 3, p. 294, doi. 10.1111/pan.12101

By:

Jimenez, Nathalia;
Song, Kit;
Lynn, Anne M.;
Polaner, David

Publication type:

Article

Urinary prostaglandin D2 and E2 metabolites are elevated with disease severity in patients with Fukuyama congenital muscular dystrophy.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-91539-2

By:

Ishigaki, Keiko;
Takeuchi, Atsuko;
Taniguchi-Ikeda, Mariko;
Sato, Takatoshi;
Murakami, Terumi;
Shichiji, Minobu;
Ishiguro, Kumiko;
Kihara, Yuki;
Nagata, Satoru;
Urade, Yoshihiro

Publication type:

Article

Urinary prostaglandin D2 and E2 metabolites are elevated with disease severity in patients with Fukuyama congenital muscular dystrophy.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-91539-2

By:

Ishigaki, Keiko;
Takeuchi, Atsuko;
Taniguchi-Ikeda, Mariko;
Sato, Takatoshi;
Murakami, Terumi;
Shichiji, Minobu;
Ishiguro, Kumiko;
Kihara, Yuki;
Nagata, Satoru;
Urade, Yoshihiro

Publication type:

Article

Distinct muscle regenerative capacity of human induced pluripotent stem cell-derived mesenchymal stromal cells in Ullrich congenital muscular dystrophy model mice.

Published in:

Stem Cell Research & Therapy, 2024, v. 15, n. 1, p. 1, doi. 10.1186/s13287-024-03951-6

By:

Yokomizo-Goto, Megumi;
Takenaka-Ninagawa, Nana;
Zhao, Chengzhu;
Bourgeois Yoshioka, Clémence Kiho;
Miki, Mayuho;
Motoike, Souta;
Inada, Yoshiko;
Zujur, Denise;
Theoputra, William;
Jin, Yonghui;
Toguchida, Junya;
Ikeya, Makoto;
Sakurai, Hidetoshi

Publication type:

Article

Clinical features and LAMA2 mutations of patients with congenital muscular dystrophy type 1A: a case report and literature review.

Published in:

Chinese Journal of Contemporary Pediatrics, 2020, v. 22, n. 6, p. 608, doi. 10.7499/j.issn.1008-8830.2001102

By:

GUO Li;
TANG Wen-Min;
SONG Yuan-Zong

Publication type:

Article

Unexpected partial RNA deletion by two different novel COL6A2 mutations leads to Ullrich congenital muscular dystrophy.

Published in:

QJM: An International Journal of Medicine, 2024, v. 117, n. 1, p. 61, doi. 10.1093/qjmed/hcad209

By:

Xu, S;
Li, L;
Shen, L;
Wang, X;
Feng, W;
Liu, S

Publication type:

Article

Congenital muscular dystrophy: from muscle to brain.

Published in:

Italian Journal of Pediatrics, 2016, v. 42, p. 1, doi. 10.1186/s13052-016-0289-9

By:

Falsaperla, Raffaele;
Praticò, Andrea D.;
Ruggieri, Martino;
Parano, Enrico;
Rizzo, Renata;
Corsello, Giovanni;
Vitaliti, Giovanna;
Pavone, Piero

Publication type:

Article

Preliminary reliability and validity of the PedsQL™ Family Impact Module in parents of children with congenital muscular dystrophy.

Published in:

Journal of Rare Diseases, 2024, v. 3, n. 1, p. 1, doi. 10.1007/s44162-024-00057-8

By:

Lim, Yoonjeong;
Lee, Seungmin;
Hong, Ickpyo;
Han, Areum

Publication type:

Article

Anästhesie bei einer thoraxchirurgischen Patientin mit kongenitaler Muskeldystrophie Typ Ullrich.

Published in:

Die Anaesthesiologie, 2022, v. 71, n. 10, p. 784, doi. 10.1007/s00101-022-01124-9

By:

Hachenberg, Thomas;
Walles, Thorsten;
Lücke, Eva;
Schilling, Thomas

Publication type:

Article

Compression of the respiratory tract in Fukuyama congenital muscular dystrophy.

Published in:

Neurology & Clinical Neuroscience, 2018, v. 6, n. 4, p. 115, doi. 10.1111/ncn3.12194

By:

Mitsutake, Akihiko;
Matsumoto, Hideyuki;
Hatano, Keiko;
Hashida, Hideji

Publication type:

Article

Congenital muscular dystrophy with inflammation: Diagnostic considerations.

Published in:

Annals of Indian Academy of Neurology, 2016, v. 19, n. 3, p. 356, doi. 10.4103/0972-2327.186814

By:

Konkay, Kaumudi;
Angamuthu Kannan, Meena;
Lingappa, Lokesh;
Uppin, Megha S.;
Challa, Sundaram

Publication type:

Article

A case of Fukuyama congenital muscular dystrophy associated with negative electroretinograms.

Published in:

2010

By:

Kondo, Hiroyuki;
Saito, Kayoko;
Urano, Mari;
Sagara, Yukiko;
Uchio, Eiichi;
Kondo, Mineo

Publication type:

Letter

Urinary prostaglandin D2 and E2 metabolites are elevated with disease severity in patients with Fukuyama congenital muscular dystrophy.

Published in:

Scientific Reports, 2025, v. 15, n. 1, p. 1, doi. 10.1038/s41598-025-91539-2

By:

Ishigaki, Keiko;
Takeuchi, Atsuko;
Taniguchi-Ikeda, Mariko;
Sato, Takatoshi;
Murakami, Terumi;
Shichiji, Minobu;
Ishiguro, Kumiko;
Kihara, Yuki;
Nagata, Satoru;
Urade, Yoshihiro

Publication type:

Article

Megaconial congenital muscular dystrophy: Importance of cutaneous features and successful response to ustekinumab.

Published in:

Pediatric Dermatology, 2025, v. 42, n. 1, p. 118, doi. 10.1111/pde.15716

By:

Palacios‐Diaz, Rodolfo David;
Pozuelo‐Ruiz, Mónica;
Martínez‐Castellano, Francisco;
Évole‐Buselli, Montserrat

Publication type:

Article

Collagen-VI supplementation by cell transplantation improves muscle regeneration in Ullrich congenital muscular dystrophy model mice.

Published in:

Stem Cell Research & Therapy, 2021, v. 12, n. 1, p. 1, doi. 10.1186/s13287-021-02514-3

By:

Nana Takenaka-Ninagawa;
Jinsol Kim;
Mingming Zhao;
Masae Sato;
Tatsuya Jonouchi;
Megumi Goto;
Clémence Kiho Bourgeois Yoshioka;
Rukia Ikeda;
Aya Harada;
Takahiko Sato;
Makoto Ikeya;
Akiyoshi Uezumi;
Masashi Nakatani;
Satoru Noguchi;
Hidetoshi Sakurai

Publication type:

Article