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  1. Article: Deficit congenito di fattore V ed emorragia intraventricolare di origine prenatale.

    Bonvini, G / Cotta-Ramusino, A / Ricciardi, G

    La Pediatria medica e chirurgica : Medical and surgical pediatrics

    1994  Volume 16, Issue 1, Page(s) 93–94

    Abstract: The Authors describe a case of congenital coagulation factor V deficiency with severe prenatal intraventricular hemorrhage. Factor V is an essential enzyme catalysing the process of thrombin generation. Low levels of enzyme were also found in both ... ...

    Title translation Congenital factor V deficiency and intraventricular hemorrhage of prenatal origin.
    Abstract The Authors describe a case of congenital coagulation factor V deficiency with severe prenatal intraventricular hemorrhage. Factor V is an essential enzyme catalysing the process of thrombin generation. Low levels of enzyme were also found in both parents, who demonstrate subclinic alterations of coagulation parameters. The severe deficiency of factor V in the newborn (8%) caused frequent and severe intracranial and gastric hemorrhages that brought newborn to death in few weeks.
    MeSH term(s) Blood Coagulation Tests ; Cerebral Hemorrhage/etiology ; Factor V Deficiency/complications ; Factor V Deficiency/diagnosis ; Fetal Diseases ; Gastrointestinal Hemorrhage/etiology ; Hematoma, Subdural/etiology ; Humans ; Infant, Newborn ; Magnetic Resonance Imaging ; Male
    Language Italian
    Publishing date 1994-01
    Publishing country Italy
    Document type Case Reports ; English Abstract ; Journal Article
    ZDB-ID 605942-9
    ISSN 2420-7748 ; 0391-5387
    ISSN (online) 2420-7748
    ISSN 0391-5387
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

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  2. Article: La sindrome della displasia ectodermica ipoidrotica. Descrizione di un caso clinico.

    Bonvini, G / Cotta-Ramusino, A / Pagliano-Sassi, L

    La Pediatria medica e chirurgica : Medical and surgical pediatrics

    1989  Volume 11, Issue 4, Page(s) 467–469

    Abstract: A case of Hypohidrotic Ectodermal Dysplasia is reported. Inability of sweating is associated with characteristic craniofacial anomalies, oligo-anodontia and rare, thin hair. X-linked and autosomal inheritance are both supposed. ...

    Title translation Hypohidrotic ectodermal dysplasia syndrome. Description of a clinical case.
    Abstract A case of Hypohidrotic Ectodermal Dysplasia is reported. Inability of sweating is associated with characteristic craniofacial anomalies, oligo-anodontia and rare, thin hair. X-linked and autosomal inheritance are both supposed.
    MeSH term(s) Anodontia ; Ectodermal Dysplasia/genetics ; Humans ; Infant ; Male ; Phenotype ; Syndrome
    Language Italian
    Publishing date 1989-07
    Publishing country Italy
    Document type Case Reports ; English Abstract ; Journal Article ; Review
    ZDB-ID 605942-9
    ISSN 2420-7748 ; 0391-5387
    ISSN (online) 2420-7748
    ISSN 0391-5387
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: Sindrome di William-Beuren: descrizione di un caso.

    Bonvini, G / Cotta-Ramusino, A / Ricciardi, G / Pagliano-Sassi, L

    La Pediatria medica e chirurgica : Medical and surgical pediatrics

    1991  Volume 13, Issue 5, Page(s) 519–522

    Abstract: The Authors describe a case of William-Beuren Syndrome, also know as "Fanconi-Schlesinger Syndrome" or "Idiopathic Hypercalcaemia, supravalvular aortic stenosis, elfin facies syndrome". Irritability and chronic constipation are early features. ... ...

    Title translation William-Beuren syndrome: description of a case.
    Abstract The Authors describe a case of William-Beuren Syndrome, also know as "Fanconi-Schlesinger Syndrome" or "Idiopathic Hypercalcaemia, supravalvular aortic stenosis, elfin facies syndrome". Irritability and chronic constipation are early features. Hypercalcaemia may occur in infancy but rarely after 1 year age. The facies is characteristic. Supravalvular aortic stenosis is the most frequent cardiac abnormality. Other common features are short stature, mental retardation and significant behavioural disorders. In this case report typical facies, short stature, behavioural disorders are associated with epilepsy in early years of life. Hypercalcaemia or cardiovascular malformation were not found.
    MeSH term(s) Aortic Valve Stenosis/congenital ; Aortic Valve Stenosis/diagnosis ; Face/abnormalities ; Humans ; Infant, Newborn ; Male ; Syndrome
    Language Italian
    Publishing date 1991-09
    Publishing country Italy
    Document type Case Reports ; English Abstract ; Journal Article
    ZDB-ID 605942-9
    ISSN 2420-7748 ; 0391-5387
    ISSN (online) 2420-7748
    ISSN 0391-5387
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Determinazione del fenobarbitale in sciroppi previa separazione elettroforetica su striscia.

    Bennati, E / Cotta Ramusino, A

    Il Farmaco; edizione pratica

    1970  Volume 25, Issue 4, Page(s) 253–256

    Title translation Determination of phenobarbital in syrups by strip electrophoresis.
    MeSH term(s) Electrophoresis ; Pharmaceutical Vehicles/analysis ; Phenobarbital/analysis ; Spectrophotometry
    Chemical Substances Pharmaceutical Vehicles ; Phenobarbital (YQE403BP4D)
    Language Italian
    Publishing date 1970-04
    Publishing country Italy
    Document type Journal Article
    ISSN 0430-0912
    ISSN 0430-0912
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  5. Article ; Online: Search for Lepton Number and Flavor Violation in K^{+} and π^{0} Decays.

    Aliberti, R / Ambrosino, F / Ammendola, R / Angelucci, B / Antonelli, A / Anzivino, G / Arcidiacono, R / Bache, T / Baeva, A / Baigarashev, D / Barbanera, M / Bernhard, J / Biagioni, A / Bician, L / Biino, C / Bizzeti, A / Blazek, T / Bloch-Devaux, B / Bonaiuto, V /
    Boretto, M / Bragadireanu, A M / Britton, D / Brizioli, F / Brunetti, M B / Bryman, D / Bucci, F / Capussela, T / Carmignani, J / Ceccucci, A / Cenci, P / Cerny, V / Cerri, C / Checcucci, B / Conovaloff, A / Cooper, P / Cortina Gil, E / Corvino, M / Costantini, F / Cotta Ramusino, A / Coward, D / D'Agostini, G / Dainton, J B / Dalpiaz, P / Danielsson, H / De Simone, N / Di Filippo, D / Di Lella, L / Doble, N / Duk, V / Duval, F / Döbrich, B / Emelyanov, D / Engelfried, J / Enik, T / Estrada-Tristan, N / Falaleev, V / Fantechi, R / Fascianelli, V / Federici, L / Fedotov, S / Filippi, A / Fiorini, M / Fry, J R / Fu, J / Fucci, A / Fulton, L / Gamberini, E / Gatignon, L / Georgiev, G / Ghinescu, S A / Gianoli, A / Giorgi, M / Giudici, S / Gonnella, F / Goudzovski, E / Graham, C / Guida, R / Gushchin, E / Hahn, F / Heath, H / Henshaw, J / Holzer, E B / Husek, T / Hutanu, O E / Hutchcroft, D / Iacobuzio, L / Iacopini, E / Imbergamo, E / Jenninger, B / Jerhot, J / Jones, R W L / Kampf, K / Kekelidze, V / Kholodenko, S / Khoriauli, G / Khotyantsev, A / Kleimenova, A / Korotkova, A / Koval, M / Kozhuharov, V / Kucerova, Z / Kudenko, Y / Kunze, J / Kurochka, V / Kurshetsov, V / Lamanna, G / Lanfranchi, G / Lari, E / Latino, G / Laycock, P / Lazzeroni, C / Lehmann Miotto, G / Lenti, M / Leonardi, E / Lichard, P / Litov, L / Lollini, R / Lomidze, D / Lonardo, A / Lubrano, P / Lupi, M / Lurkin, N / Madigozhin, D / Mannelli, I / Mapelli, A / Marchetto, F / Marchevski, R / Martellotti, S / Massarotti, P / Massri, K / Maurice, E / Medvedeva, M / Mefodev, A / Menichetti, E / Migliore, E / Minucci, E / Mirra, M / Misheva, M / Molokanova, N / Moulson, M / Movchan, S / Napolitano, M / Neri, I / Newson, F / Norton, A / Noy, M / Numao, T / Obraztsov, V / Ostankov, A / Padolski, S / Page, R / Palladino, V / Parenti, A / Parkinson, C / Pedreschi, E / Pepe, M / Perrin-Terrin, M / Peruzzo, L / Petrov, P / Petrov, Y / Petrucci, F / Piandani, R / Piccini, M / Pinzino, J / Polenkevich, I / Pontisso, L / Potrebenikov, Yu / Protopopescu, D / Raggi, M / Romano, A / Rubin, P / Ruggiero, G / Ryjov, V / Salamon, A / Santoni, C / Saracino, G / Sargeni, F / Schuchmann, S / Semenov, V / Sergi, A / Shaikhiev, A / Shkarovskiy, S / Soldi, D / Sozzi, M / Spadaro, T / Spinella, F / Sturgess, A / Sugonyaev, V / Swallow, J / Trilov, S / Valente, P / Velghe, B / Venditti, S / Vicini, P / Volpe, R / Vormstein, M / Wahl, H / Wanke, R / Wrona, B / Yushchenko, O / Zamkovsky, M / Zinchenko, A

    Physical review letters

    2021  Volume 127, Issue 13, Page(s) 131802

    Abstract: Searches for the lepton number violating K^{+}→π^{-}μ^{+}e^{+} decay and the lepton flavor violating K^{+}→π^{+}μ^{-}e^{+} and π^{0}→μ^{-}e^{+} decays are reported using data collected by the NA62 experiment at CERN in 2017-2018. No evidence for these ... ...

    Abstract Searches for the lepton number violating K^{+}→π^{-}μ^{+}e^{+} decay and the lepton flavor violating K^{+}→π^{+}μ^{-}e^{+} and π^{0}→μ^{-}e^{+} decays are reported using data collected by the NA62 experiment at CERN in 2017-2018. No evidence for these decays is found and upper limits of the branching ratios are obtained at 90% confidence level: B(K^{+}→π^{-}μ^{+}e^{+})<4.2×10^{-11}, B(K^{+}→π^{+}μ^{-}e^{+})<6.6×10^{-11} and B(π^{0}→μ^{-}e^{+})<3.2×10^{-10}. These results improve by 1 order of magnitude over previous results for these decay modes.
    Language English
    Publishing date 2021-10-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 208853-8
    ISSN 1079-7114 ; 0031-9007
    ISSN (online) 1079-7114
    ISSN 0031-9007
    DOI 10.1103/PhysRevLett.127.131802
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Effect of a single daily dose treatment of fenofibrate on plasma lipoproteins in hyperlipoproteinaemia IIb.

    Bertolini, S / Elicio, N / Daga, A / Degl'Innocenti, M L / Balestreri, R / Fusi, M G / Cotta Ramusino, A M / Carozzi, A

    European journal of clinical pharmacology

    1988  Volume 34, Issue 1, Page(s) 25–28

    Abstract: The safety and efficacy of a single daily dose of fenofibrate (200 mg) have been evaluated in 12 Type IIB hyperlipidaemic patients in a three-month study. At the same time the pharmacokinetics was studied to check whether this new dosage schedule would ... ...

    Abstract The safety and efficacy of a single daily dose of fenofibrate (200 mg) have been evaluated in 12 Type IIB hyperlipidaemic patients in a three-month study. At the same time the pharmacokinetics was studied to check whether this new dosage schedule would give a therapeutic plasma levels of fenofibrate. At the single daily dose of 200 mg, fenofibrate was highly effective, very well tolerated, and it reached therapeutic plasma levels without accumulation. It appears that fenofibrate can usefully be employed at this dosage in hyperlipidaemia, especially since patient compliance is better when only one daily dose need be taken.
    MeSH term(s) Adult ; Anticholesteremic Agents/administration & dosage ; Anticholesteremic Agents/blood ; Anticholesteremic Agents/pharmacokinetics ; Anticholesteremic Agents/therapeutic use ; Capsules ; Clinical Trials as Topic ; Drug Administration Schedule ; Female ; Fenofibrate/administration & dosage ; Fenofibrate/analogs & derivatives ; Fenofibrate/blood ; Fenofibrate/pharmacokinetics ; Fenofibrate/therapeutic use ; Humans ; Hyperlipoproteinemia Type II/blood ; Hyperlipoproteinemia Type II/drug therapy ; Hypolipidemic Agents/administration & dosage ; Hypolipidemic Agents/blood ; Hypolipidemic Agents/pharmacokinetics ; Hypolipidemic Agents/therapeutic use ; Lipoproteins/blood ; Male ; Middle Aged ; Patient Compliance ; Propionates/administration & dosage
    Chemical Substances Anticholesteremic Agents ; Capsules ; Hypolipidemic Agents ; Lipoproteins ; Propionates ; fenofibric acid (BGF9MN2HU1) ; Fenofibrate (U202363UOS)
    Language English
    Publishing date 1988
    Publishing country Germany
    Document type Clinical Trial ; Journal Article
    ZDB-ID 121960-1
    ISSN 1432-1041 ; 0031-6970
    ISSN (online) 1432-1041
    ISSN 0031-6970
    DOI 10.1007/bf01061412
    Database MEDical Literature Analysis and Retrieval System OnLINE

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