Works matching IS 03406199 AND DT 2002 AND VI 161 AND IP 3

Results: 16

Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype.

Published in:

European Journal of Pediatrics, 2002, v. 161, n. 3, p. 169, doi. 10.1007/s00431-002-0920-1

By:

St ö ckler-Ipsiroglu, Sylvia;
Strobl, Wolfgang;
M ö slinger, Dorothea

Publication type:

Article

Children with profound biotinidase deficiency should be treated with biotin regardless of their residual enzyme activity or genotype.

Published in:

2002

By:

Wolf, Barry

Publication type:

commentary

Growth, developmental milestones and health problems in the first 2 years in very preterm infants compared with term infants: a population based study.

Published in:

2002

By:

Bucher, Hans Ulrich;
Killer, Christa;
Ochsner, Yvonne;
Vaihinger, Svantje;
Fauchere, Jean-Claude;
Fauchère, Jean-Claude

Publication type:

journal article

Congenital hemihypertrophy and pheochromocytoma, not a coincidental combination?

Published in:

2002

By:

van den Akker, Erica L.T.;
de Krijger, Ronald R.;
de Herder, Wouter W.;
Drop, Stenvert L.S.

Publication type:

journal article

Acute myeloid leukemia presenting with diabetes insipidus.

Published in:

European Journal of Pediatrics, 2002, v. 161, n. 3, p. 161, doi. 10.1007/s00431-001-0897-1

By:

Wossmann, Willi;
Borkhardt, Arndt;
Gossen, Regina;
Gobel, Franz-Josef;
Reiter, Alfred

Publication type:

Article

Acute rheumatic fever in a patient with glycogen storage disease type Ib: causal or coincidental simultaneous occurrence?

Published in:

2002

By:

Ndagijimana, Jennifer;
Niehues, Tim;
Wendel, Udo;
Schroten, Horst

Publication type:

journal article

Tuberculous pericarditis in an infant evolving during triple chemotherapy.

Published in:

European Journal of Pediatrics, 2002, v. 161, n. 3, p. 138, doi. 10.1007/s00431-001-0894-4

By:

Burg, Jochen Mey;
Schmidt, Klaus G.;
Nutzenadel, Walter;
Bettendorf, Markus

Publication type:

Article

Long-term clinical effectiveness of an acellular pertussis component vaccine and a whole cell pertussis component vaccine.

Published in:

2002

By:

Lugauer, Siegfried;
Heininger, Ulrich;
Cherry, James D.;
Stehr, Klemens

Publication type:

journal article

The effectiveness of octreotide in the treatment of post-operative chylothorax.

Published in:

2002

By:

Rosti, Luca;
M. Bini, Roberta;
Chessa, Massimo;
Butera, Gianfranco;
Drago, Manuela;
Carminati, Mario;
Bini, Roberta M

Publication type:

journal article

Familial 22q11.2 deletion: an infant with interrupted aortic arch and DiGeorge syndrome delivered from by a mother with tetralogy of Fallot.

Published in:

2002

By:

Ito, Tadahiko;
Okubo, Tadashi;
Sato, Hiroshi

Publication type:

Case Study

Cerebrospinal fluid levels of cytokines and soluble tumour necrosis factor receptor in acute disseminated encephalomyelitis.

Published in:

2002

By:

Ichiyama, Takashi;
Shoji, Hiroshi;
Kato, Mitsuhiro;
Sawaishi, Yukio;
Ozawa, Hiroshi;
Matsubara, Tomoyo;
Furukawa, Susumu

Publication type:

journal article

Hyperammonaemic encephalopathy in a 13-year-old boy.

Published in:

2002

By:

Laube, Guido F.;
Superti-Furga, Andrea;
Losa, Michele;
Buttiker, Vera;
Berger, Christoph;
Neuhaus, Thomas J.;
Büttiker, Vera

Publication type:

journal article

Epidemiology of Streptococcus pneumoniae pharyngeal carriage among healthy Turkish infants and children.

Published in:

2002

By:

Bakir, Mustafa;
Yagci, Aysegul;
Akbenlioglu, Cengiz;
Ilki, Arzu;
Ulger, Nurver;
Soyletir, Guner

Publication type:

Letter

Mydriasis due to self-administered inhaled ipratropium bromide.

Published in:

2002

By:

Bond, David W.;
Vyas, Harish;
Venning, Helen E.

Publication type:

Letter

Cerebellar hypoplasia, hypergonadotrophic hypogonadism, retinitis pigmentosa, alopecia, microcephaly, psychomotor retardation, and short stature: "D-CHRAMPS syndrome".

Published in:

2002

By:

Hiyasat, Dana;
Dehyyat, Munir A.;
Ajlouni, Salch;
Mubaidin, Ammar F.;
Till, Maha;
Hadidi, Azmi;
El-Shanti, Hatem;
Ajlouni, Kamel M.;
Ajlouni, Saleh

Publication type:

Case Study

Clinical heterogeneity in eyelid myoclonia, with absences, and epilepsy.

Published in:

2002

By:

Incorpora, Gemma;
Sofia, Vito;
Pavone, Piero;
Biondi, Roberto;
Barone, Baldo;
Parano, Enrico

Publication type:

Letter