Search Results - "Sbolgi, P"

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  1. 1
    Juvenile fibromyalgia syndrome: 2 clinical cases

    Juvenile fibromyalgia syndrome: 2 clinical cases by Saccomani, L, Vigliarolo, M A, Sbolgi, P, Ruffa, G, Doria Lamba, L

    Published in La Pediatria medica e chirurgica (01-01-1993)
    “…We report two cases (F. 11 years, M. 7 years) with juvenile fibro-myalgic syndrome, diagnosed because of the presence of musculo-skeletal pain, tender points…”
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  2. 2
    The Bartter-like syndrome in 2 twins

    The Bartter-like syndrome in 2 twins by Ruffa, G, Vigliarolo, M A, Sbolgi, P, Milanaccio, C

    Published in Minerva pediatrica (01-07-1993)
    “…We present a case of two twins, admitted to our department at the age of 9 years and 9 months for poor stature-ponderal growth. Hematochemical tests showed…”
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  3. 3
    The Fanconi-Bickel syndrome: one more case

    The Fanconi-Bickel syndrome: one more case by Ruffa, G, Ferrando, M, Sbolgi, P, Bartolozzi, G, Lavia, N

    Published in Minerva pediatrica (01-06-1992)
    “…The association of de Toni-Debré-Fanconi syndrome with alteration of galactose metabolism and glycogen hepatic storage, before further clarification, is…”
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  4. 4
    Renovascular hypertension-bilateral kidney: autotransplantation and reconstruction of the aorta with autologous saphena

    Renovascular hypertension-bilateral kidney: autotransplantation and reconstruction of the aorta with autologous saphena by Ruffa, G, Valente, V, Sbolgi, P, Cariati, M, Arcuri, V, Grandinetti, A, Nigro, M

    Published in Minerva pediatrica (01-04-1995)
    “…The authors describe a patient with stenosis of the renal artery undergoing bilateral kidney autotransplantation and reconstruction of the aorta with…”
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  5. 5
    Osteopetrosis and renal acidosis: a new case of this rare syndrome

    Osteopetrosis and renal acidosis: a new case of this rare syndrome by Ruffa, G, Milanaccio, C, Sbolgi, P, Levato, G L, Bartocci, M, Galasso, V, Bruschettini, P L

    Published in Minerva pediatrica (01-04-1995)
    “…The association between osteopetrosis and renal acidosis is not accidental, but represents a well-known syndrome with autosomal recessive transmission, due to…”
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  6. 6
    Anti-gliadin antibodies in the diagnosis and follow-up of celiac disease

    Anti-gliadin antibodies in the diagnosis and follow-up of celiac disease by Sbolgi, P, Mangiante, G, Ruffa, G, Caprioli, F, Bartolozzi, G, Cingolani, M, Gemme, G

    Published in Minerva pediatrica (01-12-1991)
    “…The study assessed the value of anti-gliadin antibodies (AGA) as a diagnostic test for celiac disease (CD) by examining 219 children: 57 were affected by…”
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  7. 7
    The "Charlie M." syndrome: a new clinical entity? Description of a case

    The "Charlie M." syndrome: a new clinical entity? Description of a case by Bonioli, E, Sbolgi, P, Bernaola, E, Pacciani, G, Cottafava, F

    Published in Minerva pediatrica (31-05-1980)
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  8. 8
    Smith-Lemli-Opitz syndrome. Description of 2 cases and review of the literature

    Smith-Lemli-Opitz syndrome. Description of 2 cases and review of the literature by Gemme, G, Bonioli, E, Ruffa, G, Sbolgi, P

    Published in Minerva pediatrica (31-05-1978)
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  9. 9
    Clinical and radiological aspects of hypochondroplasia. Description of 6 cases

    Clinical and radiological aspects of hypochondroplasia. Description of 6 cases by Gemme, G, Pinelli, G, Bonioli, E, Sbolgi, P, Bonzano, M A

    Published in Minerva pediatrica (28-02-1980)
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