Citation Impact
Citing Papers
Cochrane Database of Systematic Reviews
2003 Standout
Pathophysiology of acute wound healing
2007 Standout
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies
2001
Nonmuscular involvement in merosin-negative congenital muscular dystrophy
2002
Laminins during muscle development and in muscular dystrophies
1999
Mild Congenital Muscular Dystrophy in Two Patients with an Internally Deleted Laminin 2-Chain
1997
LAMA2 stop-codon mutation: Merosin-deficient congenital muscular dystrophy with occipital polymicrogyria, epilepsy and psychomotor regression
2008
The microenvironment of the embryonic neural stem cell: Lessons from adult niches?
2007
Laminins and human disease
2000
Primary myopathies and the heart
2008
New FKRP mutations causing congenital muscular dystrophy associated with mental retardation and central nervous system abnormalities. Identification of a founder mutation in Tunisian families
2004
Glycosylation in Cellular Mechanisms of Health and Disease
2006 Standout
Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families
1996
The muscular dystrophies
2002 Standout
Angiogenesis: an organizing principle for drug discovery?
2007 Standout
Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study
2011 Standout
Diagnosis and management of cricopharyngeal achalasia and other upper esophageal sphincter opening disorders
2000
Gastrostomy placement in paediatric patients with neuromuscular disorders: indications and outcome
2007
Prevalence of Muscular Dystrophies: A Systematic Literature Review
2014 Standout
Muscular dystrophies
2013
Mild muscular dystrophy due to a nonsense mutation in the LAMA2 gene resulting in exon skipping
2001
A systematic review of population based epidemiological studies in Myasthenia Gravis
2010 Standout
Human Splicing Finder: an online bioinformatics tool to predict splicing signals
2009 Standout
Patterns of laminins and integrins in the embryonic ventricular zone of the CNS
2007
Mutations in the integrin α7 gene cause congenital myopathy
1998
β1 Integrin Maintains Integrity of the Embryonic Neocortical Stem Cell Niche
2009
Immunohistological intensity measurements as a tool to assess sarcolemma‐associated protein expression
2009
The expanding phenotype of laminin α2 chain (merosin) abnormalities: case series and review
2001
Congenital muscular dystrophy with merosin deficiency: MRI findings in five patients
1998
Congenital muscular dystrophies: New aspects of an expanding group of disorders
2006
Immunocytochemical analysis of human muscular dystrophy
2000
Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy
1996
Congenital Muscular Dystrophy With Complete Laminin-α2-Deficiency, Cortical Dysplasia, and Cerebral White-Matter Changes in Children
1998
Congenital Muscular Dystrophy in Arab Children
2006
Applications of the Morris water maze in the study of learning and memory
2001 Standout
The muscular dystrophies
2012
ADHESION MOLECULES AND INHERITED DISEASES OF THE HUMAN NERVOUS SYSTEM
1998
Fiber Types in Mammalian Skeletal Muscles
2011 Standout
Cardiac Involvement in Fukuyama-type Congenital Muscular Dystrophy
2006
Congenital muscular dystrophy with rigid spine syndrome: A clinical, pathological, radiological, and genetic study
2000
Satellite Cells and the Muscle Stem Cell Niche
2013 Standout
A unique microvascular phenotype shared by juvenile hemangiomas and human placenta.
2001
Transcriptomes of germinal zones of human and mouse fetal neocortex suggest a role of extracellular matrix in progenitor self-renewal
2012 StandoutNobel
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Vascular Anomalies Classification: Recommendations From the International Society for the Study of Vascular Anomalies
2015 Standout
Works of J. Philpot being referenced
Cognitive abilities in children with congenital muscular dystrophy: correlation with brain MRI and merosin status
1999
Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy
1995
Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal
1995
Feeding problems in merosin deficient congenital muscular dystrophy
1999
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy
1996
Evidence of left ventricular dysfunction in children with merosin-deficient congenital muscular dystrophy
1998
Laminin α2-chain gene mutations in two siblings presenting with limb-girdle muscular dystrophy
1998
Expression of laminin subunits in congenital muscular dystrophy
1995
Somatosensory and Visual Evoked Potentials in Congenital Muscular Dystrophy: Correlation with MRI Changes and Muscle Merosin Status
1995
Minor Neurological and Perceptuo-Motor Deficits in Children with Congenital Muscular Dystrophy: Correlation with Brain MRI Changes
1995
Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.
1997
Merosin-deficient congenital muscular dystrophy: the spectrum of brain involvement on magnetic resonance imaging
1999