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Leonardo Murgiano
(L Murgiano)
ORCID
Publication Activity (10 Years)
Years Active: 2020-2024
Publications (10 Years): 6
Top Topics
Mass Spectrometry
Emergency Department
Iron Deficiency
Intellectual Disability
Top Venues
G3 (Bethesda, Md.)
Animal genetics
Movement disorders : official journal of the Movement Disorder Society
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This page only lists publications with an associated author ORCID identifier.
Publications
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Leonardo Murgiano
,
Esha Banjeree
,
Cynthia O'Connor
,
Keiko Miyadera
,
Petra Werner
,
Jessica K Niggel
,
Gustavo D Aguirre
,
Margret L Casal
A naturally occurring canine model of syndromic congenital microphthalmia.
G3 (Bethesda, Md.)
14 (6) (2024)
Leonardo Murgiano
,
Esha Banjeree
,
Cynthia O'Connor
,
Keiko Miyadera
,
Petra Werner
,
Jessica K Niggel
,
Gustavo D Aguirre
,
Margret L Casal
A naturally occurring canine model of syndromic congenital microphthalmia.
G3 (Bethesda, Md.)
14 (6) (2024)
Shawna R Cook
,
Cleo Schwarz
,
Julien Guevar
,
Charles-Antoine Assenmacher
,
Maeve Sheehy
,
Nathan Fanzone
,
Molly E Church
,
Leonardo Murgiano
,
Margret L Casal
,
Vidhya Jagannathan
,
Rodrigo Gutierrez Quintana
,
Mark Lowrie
,
Frank Steffen
,
Tosso Leeb
,
Kari J Ekenstedt
Canine RNF170 Single Base Deletion in a Naturally Occurring Model for Human Neuroaxonal Dystrophy.
Movement disorders : official journal of the Movement Disorder Society
(2024)
Leonardo Murgiano
,
Esha Banjeree
,
Cynthia O'Connor
,
Keiko Miyadera
,
Petra Werner
,
Jessica K Niggel
,
Gustavo D Aguirre
,
Margret L Casal
A naturally occurring canine model of syndromic congenital microphthalmia.
G3 (Bethesda, Md.)
(2024)
Leonardo Murgiano
,
Esha Banjeree
,
Cynthia O'Connor
,
Keiko Miyadera
,
Petra Werner
,
Jessica K Niggel
,
Gustavo D Aguirre
,
Margret L Casal
A naturally occurring canine model of syndromic congenital microphthalmia.
G3 (Bethesda, Md.)
14 (6) (2024)
Irene Monika Häfliger
,
Anna Letko
,
Leonardo Murgiano
,
Cord Drögemüller
De novo stop-lost germline mutation in FGFR3 causes severe chondrodysplasia in the progeny of a Holstein bull.
Animal genetics
51 (3) (2020)