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PubPharm (11)
1
Fibroblasts and Endothelial Cells in Three-Dimensional Models : A New Tool for Addressing the Pathogenesis of Systemic Sclerosis as a Prototype of Fibrotic Vasculopathies
enthalten in:
International journal of molecular sciences
| 2024
von
Bodio, C.
|
Milesi, A.
|
Lonati, P.
| +6
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2
Comparison of Protein- or Amino Acid-Based Supplements in the Rehabilitation of Men with Severe Obesity : A Randomized Controlled Pilot Study
enthalten in:
Journal of clinical medicine
| 2023
von
Brunani, A.
|
Cancello, R.
|
Gobbi, M.
| +10
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3
Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy
enthalten in:
Orphanet journal of rare diseases
| 2021
von
Magliano, L.
|
Obici, L.
|
Sforzini, C.
| +37
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4
Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation
enthalten in:
Journal of the neurological sciences
| 2016
von
Pradotto, L.
|
Mencarelli, M.
|
Bigoni, M.
| +3
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5
Recurrent transient global amnesia as presenting symptoms of CADASIL
enthalten in:
Clinical case reports
| 2016
von
Pradotto, L.
|
Orsi, L.
|
Mencarelli, M.
| +5
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6
Episodic ataxia and SCA6 within the same family due to the D302N CACNA1A gene mutation
enthalten in:
Journal of the neurological sciences
| 2016
von
Pradotto, L.
|
Mencarelli, M.
|
Bigoni, M.
| +3
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7
Amyloid polyneuropathy following domino liver transplantation
enthalten in:
Muscle & nerve
| 2012
von
Pradotto, L.
|
Franchello, A.
|
Milesi, A.
| +6
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8
Amyloid polyneuropathy following domino liver transplantation
enthalten in:
Muscle & nerve
| 2012
von
Pradotto, L.
|
Franchello, A.
|
Milesi, A.
| +6
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9
A new NOTCH3 mutation presenting as primary intracerebral haemorrhage
enthalten in:
Journal of the neurological sciences
| 2012
von
Pradotto, L.
|
Orsi, L.
|
Daniele, D.
| +5
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10
A new NOTCH3 mutation presenting as primary intracerebral haemorrhage
enthalten in:
Journal of the neurological sciences
| 2012
von
Pradotto, L.
|
Orsi, L.
|
Daniele, D.
| +5
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ATTRv
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