Works matching IS 03406199 AND DT 2010 AND VI 169 AND IP 4

Results: 24

A 12-month-old boy with a localized verrucous tumor.

Published in:

2010

By:

Möhrenschlager, Matthias;
Ring, Johannnes;
Henkel, Verena;
Möhrenschlager, Matthias

Publication type:

journal article

Behçet disease: treatment of vascular involvement in children.

Published in:

2010

By:

Ozen, Seza;
Bilginer, Yelda;
Besbas, Nesrin;
Ayaz, Nuray Aktay;
Bakkaloglu, Aysin

Publication type:

journal article

Familial primary carpal tunnel syndrome with possible skipped generation.

Published in:

2010

By:

Senel, Saliha;
Ceylaner, Gulay;
Yuksel, Deniz;
Erkek, Nilgun;
Karacan, Candemir

Publication type:

journal article

Sclerosing cholangitis and combination antifungal therapy for PNP deficiency patients.

Published in:

2010

By:

Gonzalez-Granado, Luis Ignacio

Publication type:

Letter

Clinical practice: management of biliary atresia.

Published in:

2010

By:

Khalil, Basem A.;
Perera, M. Thamara P. R.;
Mirza, Darius F.

Publication type:

journal article

Prevalence of flexible flatfoot in Taiwanese school-aged children in relation to obesity, gender, and age.

Published in:

2010

By:

Jen-Huei Chang;
Sheng-Hao Wang;
Chun-Lin Kuo;
Hsian Chung Shen;
Ya-Wen Hong;
Leou-Chyr Lin;
Chang, Jen-Huei;
Wang, Sheng-Hao;
Kuo, Chun-Lin;
Shen, Hsian Chung;
Hong, Ya-Wen;
Lin, Leou-Chyr

Publication type:

journal article

Diagnosis, treatment and follow-up of 25 patients with melamine-induced kidney stones complicated by acute obstructive renal failure in Beijing Children's Hospital.

Published in:

2010

By:

Qiang Sun;
Ying Shen;
Ning Sun;
Gui Ju Zhang;
Zhi Chen;
Jian Feng Fan;
Li Qun Jia;
Hong Zhan Xiao;
Xu Ran Li;
Puschner, Birgit;
Sun, Qiang;
Shen, Ying;
Sun, Ning;
Zhang, Gui Ju;
Chen, Zhi;
Fan, Jian Feng;
Jia, Li Qun;
Xiao, Hong Zhan;
Li, Xu Ran

Publication type:

journal article

Clinical practice: heart failure in children. Part II: current maintenance therapy and new therapeutic approaches.

Published in:

2010

By:

Kantor, Paul F.;
Mertens, Luc L.

Publication type:

journal article

Involvement of tryptophan hydroxylase 2 (TPH2) gene polymorphisms in susceptibility to coronary artery lesions in Korean children with Kawasaki disease.

Published in:

2010

By:

Park, Sung Wook;
Ban, Ju Yeon;
Yoon, Kyung Lim;
Kim, Hak Jae;
Chung, Jun Young;
Yi, Jae Woo;
Lee, Bong Jae;
Chung, Joo-Ho

Publication type:

journal article

Eponym: the Lemierre syndrome.

Published in:

2010

By:

Vargiami, Efthimia G.;
Zafeiriou, D. I.

Publication type:

journal article

Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q.

Published in:

2010

By:

Pavone, Piero;
Ruggieri, Martino;
Lombardo, Ilaria;
Sudi, Jyotsna;
Biancheri, Roberta;
Castellano-Chiodo, Danilo;
Rossi, Andrea;
Incorpora, Gemma;
Nowak, Norma J.;
Christian, Susan L.;
Pavone, Lorenzo;
Dobyns, William B.

Publication type:

journal article

LEOPARD syndrome with recurrent PTPN11 mutation Y279C and different cutaneous manifestations: two case reports and a review of the literature.

Published in:

European Journal of Pediatrics, 2010, v. 169, n. 4, p. 469, doi. 10.1007/s00431-009-1058-1

By:

Kalev, Ingrid;
Muru, Kai;
Teek, Rita;
Zordania, Riina;
Reimand, Tiia;
Köbas, Kristel;
Õunap, Katrin

Publication type:

Article

A patient with Lemierre syndrome.

Published in:

2010

By:

Vargiami, Efthimia G.;
Farmaki, E.;
Tasiopoulou, D.;
Zafeiriou, D. I.;
Badouraki, M.;
Anastasiou, A.;
Karkos, C.;
Gombakis, N.;
Athanasiou-Metaxa, M.

Publication type:

journal article

Gradenigo's syndrome with lateral venous sinus thrombosis: successful conservative treatment.

Published in:

2010

By:

Scardapane, Alessandra;
Del Torto, Marianna;
Nozzi, Manuela;
Elio, Concettina;
Breda, Luciana;
Chiarelli, Francesco

Publication type:

journal article

Virilizing adrenocortical carcinoma in a child with Turner syndrome and somatic TP53 gene mutation.

Published in:

2010

By:

Ko, Jung-Hee;
Lee, Hyo Sung;
Hong, Jeong;
Hwang, Jin Soon

Publication type:

journal article

Dyschromatosis ptychotropica: an unusual pigmentary disorder in a boy with epileptic encephalopathy and progressive atrophy of the central nervous system-a novel entity?

Published in:

2010

By:

Helbig, Ingo;
Fölster-Holst, Regina;
Brasch, Jochen;
Hausser, Ingrid;
Van Baalen, Andreas;
Muhle, Hiltrud;
Alfke, Karsten;
Caliebe, Almuth;
Stephani, Ulrich;
Happle, Rudolf;
Fölster-Holst, Regina

Publication type:

journal article

Submandibular lymphadenitis caused by Mycobacterium interjectum: contribution of new diagnostic tools.

Published in:

2010

By:

Tuerlinckx, David;
Fauville-Dufaux, Maryse;
Bodart, Eddy;
Bogaerts, Pierre;
Dupont, Bernadette;
Glupczynski, Youri;
Glupeczynski, Youri

Publication type:

journal article

Reply to correspondence letter by Luis Ignacio Gonzalez-Granado.

Published in:

2010

By:

Aytekin, Caner;
Dogu, Figen;
Ikinciogullari, Aydan

Publication type:

Letter

Ochoa syndrome: a spectrum of urofacial syndrome.

Published in:

2010

By:

Aydogdu, Ozgu;
Burgu, Berk;
Demirel, Fuat;
Soygur, Tarkan;
Ozcakar, Zeynep Birsin;
Yalcınkaya, Fatos;
Tekgul, Serdar;
Yalcinkaya, Fatos

Publication type:

journal article

A novel L1CAM mutation in a fetus detected by prenatal diagnosis.

Published in:

2010

By:

Piccione, Maria;
Matina, Federico;
Fichera, Marco;
Giudice, Mariangela Lo;
Damiani, Gianfranca;
Jakil, Maria Cristina;
Corsello, Giovanni;
Lo Giudice, Mariangela

Publication type:

journal article

Rapid diagnosis of herpetic encephalitis in children by PCR-microarray technology for simultaneous detection of seven human herpes viruses.

Published in:

2010

By:

Jianrong Shi;
Yidong Wu;
Meiting Cai;
Shiqiang Shang;
Shi, Jianrong;
Wu, Yidong;
Cai, Meiting;
Shang, Shiqiang

Publication type:

journal article

Non-accidental chlorpyrifos poisoning-an unusual cause of profound unconsciousness.

Published in:

2010

By:

Jiun-Chang Lee;
Kuang-Lin Lin;
Jainn-Jim Lin;
Shao-Hsuan Hsia;
Chang-Teng Wu;
Lee, Jiun-Chang;
Lin, Kuang-Lin;
Lin, Jainn-Jim;
Hsia, Shao-Hsuan;
Wu, Chang-Teng

Publication type:

journal article

A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum.

Published in:

2010

By:

Koehler, Udo;
Holinski-Feder, Elke;
Ertl-Wagner, Birgit;
Kunz, Juergen;
Von Moers, Arpad;
Von Voss, Hubertus;
Schell-Apacik, Chayim

Publication type:

journal article

Mycoplasma pneumoniae associated opsoclonus-myoclonus syndrome in three cases.

Published in:

2010

By:

Huber, Benedikt Maria;
Strozzi, Susi;
Steinlin, Maja;
Aebi, Christoph;
Fluri, Simon

Publication type:

journal article