|
🐜
|
Nonalcoholic steatohepatitis: association of insulin resistance and mitochondrial abnormalities.
9 auth.
A. Sanyal,
Carol Campbell-Sargent,
F. Mirshahi,
W. Rizzo,
M. Contos,
R. Sterling,
...
V. Luketic,
M. Shiffman,
J. Clore
|
11 |
2001 |
11
🐜
|
|
🐜
|
Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy
37 auth.
A. Biffi,
E. Montini,
L. Lorioli,
M. Cesani,
F. Fumagalli,
T. Plati,
C. Baldoli,
S. Martino,
A. Calabria,
Sabrina Canale,
F. Benedicenti,
G. Vallanti,
L. Biasco,
Simone Leo,
N. Kabbara,
...
G. Zanetti,
W. Rizzo,
Nalini A. L. Mehta,
M. Cicalese,
Miriam Casiraghi,
J. Boelens,
U. Del Carro,
D. Dow,
M. Schmidt,
A. Assanelli,
Victor Neduva,
C. Di Serio,
E. Stupka,
J. Gardner,
C. von Kalle,
C. Bordignon,
F. Ciceri,
A. Rovelli,
M. Roncarolo,
A. Aiuti,
M. Sessa,
L. Naldini
|
10 |
2013 |
10
🐜
|
|
🐢
|
Mitochondrial fatty-acid oxidation disorders.
Michelle Kompare,
W. Rizzo
|
8 |
2008 |
8
🐢
|
|
🐢
|
Sjögren–Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase gene
8 auth.
V. Laurenzi,
G. Rogers,
David J Hamrock,
L. Marekov,
P. Steinert,
J. Compton,
...
N. Markova,
W. Rizzo
|
8 |
1996 |
8
🐢
|
|
🐜
|
Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines.
11 auth.
N. Braverman,
G. Raymond,
W. Rizzo,
A. Moser,
M. Wilkinson,
E. Stone,
...
S. Steinberg,
M. Wangler,
E. Rush,
J. Hacia,
Mousumi Bose
|
7 |
2016 |
7
🐜
|
|
🦁
|
Dietary erucic acid therapy for X‐linked adrenoleukodystrophy
10 auth.
W. Rizzo,
R. Leshner,
A. Odone,
A. Dammann,
D. Craft,
M. Jensen,
...
S. Jennings,
S. Davis,
R. Jaitly,
J. Sgro
|
7 |
1989 |
7
🦁
|
|
🐜
|
Recessive mutations in ELOVL4 cause ichthyosis, intellectual disability, and spastic quadriplegia.
8 auth.
Mohammed A. Aldahmesh,
Jawahir Y. Mohamed,
Hisham S. Alkuraya,
I. Verma,
R. Puri,
A. Alaiya,
...
W. Rizzo,
F. Alkuraya
|
7 |
2011 |
7
🐜
|
|
🐜
|
A clinical approach to the diagnosis of patients with leukodystrophies and genetic leukoencephelopathies.
14 auth.
S. Parikh,
G. Bernard,
R. Leventer,
M. S. van der Knaap,
J. V. Van Hove,
A. Pizzino,
N. McNeill,
G. Helman,
Cas Simons,
Johanna L Schmidt,
...
W. Rizzo,
M. Patterson,
R. Taft,
A. Vanderver
|
7 |
2015 |
7
🐜
|
|
🦁
|
Sjögren-Larsson syndrome: molecular genetics and biochemical pathogenesis of fatty aldehyde dehydrogenase deficiency.
W. Rizzo
|
7 |
2007 |
7
🦁
|
|
🦁
|
Adrenoleukodystrophy
W. Rizzo,
P. Watkins,
M. Phillips,
Debra Cranin,
B. Campbell,
J. Avigan
|
7 |
1986 |
7
🦁
|
|
🦁
|
Sjögren‐Larsson syndrome: Diversity of mutations and polymorphisms in the fatty aldehyde dehydrogenase gene (ALDH3A2)
W. Rizzo,
G. Carney
|
6 |
2005 |
6
🦁
|
|
🦁
|
Fatty aldehyde and fatty alcohol metabolism: review and importance for epidermal structure and function.
W. Rizzo
|
6 |
2014 |
6
🦁
|
