Creatine Kinase

Un bambino con difficoltà nella deambulazione: la miosite acuta benigna dell'infanzia

Ruberto E, Scaglione F, Starita A

2025/9 — pag. 224-225 — DOI

The paper describes the case of a 5-year-old child presenting with sudden walking difficulty after influenza-like symptoms. The definitive diagnosis was based on accurate anamnesis and physical examination and a few laboratory tests: benign acute chi...

Rabdomiolisi massiva da influenza B: quando i dolori muscolari non sono una "banale influenza"

Operti M, Laccisaglia A, Feyles F, Vassia C, Peruzzi L, Conio A, Versace A

2025/1 — pag. 16-17 — DOI

A 10-year-old girl with severe rhabdomyolysis linked to type B influenza showed rapid improvement without dialysis after being treated with hydration, albumin, diuretics, N-acetylcysteine and oseltamivir. This severe case highlights the potential myo...

Crampi muscolari, iperCPKemia e fenomeno “second wind”: la malattia di McArdle

Faraguna MC, Barzaghi S, Crescitelli V, Pretese R, Fornari A, Gasperini S.

2024/1 — pag. 50-53 — DOI

The case of a 12-year-old girl presenting with poor exercise tolerance, muscular cramps and CPK high levels is described. The diagnosis of McArdle disease was eventually made due to the classic “second wind” sign....

Quando la rabdomiolisi risponde al glucosio

Di Nora A, La Spina L, Meli C, Ruggieri M.

2023/5 — pag. 331-334 — DOI

The case of an 8-year-old boy complaining easy tiredness, poor exercise tolerance and high CPK blood level is described. The diagnosis of glutaric aciduria type II was finally made....

Quando la rabdomiolisi risponde al glucosio

Di Nora A, La Spina L, Meli C, Ruggieri M

2023/5 — pag. 91-91 — DOI

The case of an 8-year-old boy complaining easy tiredness, poor exercise tolerance and high CPK blood level is described. The diagnosis of glutaric aciduria type II was finally made....

Fisiopatologia dell’ipotiroidismo acquisito

Folegatti A, Cardani R, Vergori A

2023/5 — pag. 82-86 — DOI

Acquired hypothyroidism represents a frequent challenge for paediatricians. Knowing the pathophysiological basis of this disease and its main clinical manifestations is closely linked to proper diagnostic and therapeutic management. As is well known,...

Rabdomiolisi... stellare

Belleri P, Guariento M, Tisato MG, La Fauci G.

2023/2 — pag. 127-130 — DOI

The case of a 9-year-old boy presenting with brown coloured urine (myoglobinuria) and extraordinarily high blood CPK levels is described. A diagnosis of rhabdomyolisis related to a Coxsackievirus A and B infection was finally made....

Rabdomiolisi... stellare

Belleri P, Guariento M, Tisato MG, La Fauci G

2023/2 — pag. 41-41 — DOI

The case of a 9-year-old boy presenting with brown coloured urine (myoglobinuria) and extraordinarily high blood CPK levels is described. A diagnosis of rhabdomyolisis related to a Coxsackievirus A and B infection was finally made....

Una vecchietta di quattro anni: la dermatomiosite

Gozzi A, Benelli E, Minute M, Strafella MS, Martelossi S.

2023/1 — pag. 53-54 — DOI

The Authors describe the case of a 4-year-old girl with aging appearance of the skin of her hands and feet finally diagnosed as dermatomyositis. The capillaroscopy was a crucial step in the diagnostic process....

IperCPKemia in Pediatria: approccio pratico e confronto con le linee guida

Vaivoda A, Pastore S

2023/1 — pag. 15-16 — DOI

In this retrospective, single-centre study, the Authors analyse the cause of the high blood value of the creatinphosphokinase enzyme (CPK). Even if severe diseases as muscular dystrophy are usually associated with high (> ten time normal value) blood...

IperCKemia asintomatica: la malattia di Pompe late-onset

Borelli E, Casciana ML, Salemi C, Sordelli S, Fasoli S

2021/4 — pag. 105-108 — DOI

The paper reports the case of a 7-year-old boy who presented with elevated alanine and aspartate transaminases. Further investigations demonstrated elevated creatine kinase (CK), so an underlying metabolic disorder was investigated even in absence of...

Una atassia acuta in una bambina di 15 mesi

G. Zanella, A.M.C. Galimberti

2020/3 — pag. 57-57

Il morbo di spritz… ovvero un caso di iperckemia in un ragazzo celiaco

S. Mazzoleni

2013/8

Rabdomiolisi e Mycoplasma pneumoniae: un'insolita associazione Una malattia, mille sensazioni: la mia esperienza con la fibrosi cistica

2011/3 — pag. 189-190

Rabdomiolisi in età pediatrica

C.L. Bersanini, S. Arrigoni, C. Stringhi, P. Tommasi, G. Zuin, M. Fontana

2011/3 — pag. 161-166

Rhabdomyolysis is the common final pathway of different processes that lead to the destruction of skeletal muscle and release of cellular contents in plasma; it is defined as serum creatine kinase (CK) level five times above normal in the absence o...

Distrofia muscolare di Duchenne: si può fare di più

2010/10 — pag. 663-664

Patologia quasi rara, in agguato nel nostro quotidiano. Sbagliando si impara.

2008/9 — pag. 595-596

Miosite acuta

P. Salierno, L. Calligaris

2008/8

Morsi di mezza estate

S. Stefani, E. Opocher, F. Opocher, F. Intini, V. Stritoni, L. Da Dalt

2008/6

Un Duchenne astenico

D. Sambugaro

2003/8 — pag. 532-534

La dermatomiosite giovanile

M. Lazzerini

2003/8

Distrofia muscolare: l'imbarazzo della prognosi

M. Santo

1999/2

Il tappo di cerumeIl CAF fa ancora male ai bambini?Cortisone, fitoterapia e dermatite atopicaLa promozione dell’allattamento al senoPediatria ospedaliera: la sindrome della categoria offesaCopanello, storia e ideologie: le delusioni di un pediatra ospedaliero

1999/2 — pag. 80-80