Receptors, Neurotransmitter

Un esordio psicotico misterioso

Mannone A, Minute M

2024/3 — pag. 52-52 — DOI

The authors describe the case of a 13-year-old boy presenting with a confusional state possibly due to the abuse of dextromethorphan contained in a cough syrup....

Una neonata dal “cuore matto”

Di Marco S, Rosati S, Controzzi T, Ghirri P, Peroni D

2022/9 — pag. 194-194 — DOI

The Authors describe a case of thyrotoxicosis in a newborn presenting with severe tachycardia. The diagnostic and therapeutic approach is also discussed....

Occhio normale che sporge senza trauma: pensa al Graves!

M.G. Alagna, B. Salvatore

2020/5 — pag. 111-111 — DOI

Encefalite da anticorpi anti-NMDAR

T. Granata, S. Matricardi

2014/10 — pag. 637-641

Anti-N-metyl-D-aspartate receptor (NMDAR) antibodies encephalitis is a potentially treatable disease characterized by the abrupt onset of a constellation of symptoms resulting from diffuse brain dysfunction. First described in young women as parane...

Encefalite da anticorpi anti-NMDA-R: un caso atipico

G. Mastrangelo

2014/3

Stiff-Baby Syndrome: quando pensarci. Il caso di Sofia

P. Assandro, C. Sanesi, C. Trevisol, L. Travan

2013/10

The Stiff-Baby Syndrome is a genetic startle disorder, presenting soon after birth and characterized by an exaggerated persistent startle response to unexpected stimuli and generalized muscular rigidity that decreases during sleep. Hyperekplexia is o...

La malattia di Graves-Basedow in pediatria

2011/2 — pag. 122-123

Iper-ecplexia, spasmi affettivi, ferro

2010/9 — pag. 593-594

Ipotiroidismo subclinico: dalla teoria alla pratica

C. Locatelli, M. Bensa, M. Pocecco

2005/3 — pag. 165-168

Subclinical hypothyroidism is a biochemical state characterized by an elevated serum TSH level with concomitant normal FT4 value. While in adults it frequently progresses to clinically evident hypothyroidism, in children it may be a benign and remi...

Costi e benefici in Pediatria, “p” statistico e “Confronti in Pediatria”Siparietto sulla vitamina DEpidemiologia dell’insufficienza renale cronica in ItaliaTest di immunità ritardata (Patch test), IPLV a presentazione gastrointestinale e i ricorsi storici“Vaccinate, non esitate!” (sono sempre gli Americani a parlare)RMN nella diagnosi di malattia di CrohnGenetica del comportamento: obesità, comportamento alimentare incontrollato e mutazioni del gene MC4R

2003/4 — pag. 213-214

IL DESTINO NEL DNAI geni della felicità

M.C. Fulchignoni, L. Greco

2001/1 — pag. 20-29

The genes of happiness are the best candidates for coding dopamine receptors, whereas the genes of sadness are the best candidates for coding serotonin metabolism and re-uptake. In fact, several studies on separately grown homozygous twins demonstr...