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Blepharoptosis
Known as:
Ptoses, Eyelid
, Eyelid Ptoses
, Blepharoptoses
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Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle.
National Institutes of Health
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Related topics
Related topics
50 relations
22q13.3 Deletion Syndrome
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
Aarskog syndrome
BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS (disorder)
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Narrower (4)
Blepharochalasis
Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
Mehta Lewis Patton syndrome
Ophthalmoplegia Totalis with Ptosis and Miosis
Broader (1)
Ptosis
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2005
Highly Cited
2005
A new periareolar mammaplasty: The “round block” technique
L. Benelli
Aesthetic Plastic Surgery
2005
Corpus ID: 35418572
The “round block” acts as a keystone supporting the mammary cone. The keystone lies in the dermodermic, glandulo-glandular, and…
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Highly Cited
2004
Highly Cited
2004
Ferritin Heavy Chain Upregulation by NF-κB Inhibits TNFα-Induced Apoptosis by Suppressing Reactive Oxygen Species
C. Pham
,
C. Bubici
,
+10 authors
G. Franzoso
Cell
2004
Corpus ID: 16603060
Highly Cited
2004
Highly Cited
2004
Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development.
M. Uda
,
C. Ottolenghi
,
+7 authors
G. Pilia
Human Molecular Genetics
2004
Corpus ID: 841092
FOXL2 mutations cause gonadal dysgenesis or premature ovarian failure (POF) in women, as well as eyelid/forehead dysmorphology in…
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Highly Cited
2001
Highly Cited
2001
The putative forkhead transcription factor FOXL2 is mutated in blepharophimosis/ptosis/epicanthus inversus syndrome
L. Crisponi
,
M. Deiana
,
+19 authors
G. Pilia
Nature Genetics
2001
Corpus ID: 26750194
In type I blepharophimosis/ptosis/epicanthus inversus syndrome (BPES), eyelid abnormalities are associated with ovarian failure…
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Highly Cited
1998
Highly Cited
1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy
B. Brais
,
J. Bouchard
,
+15 authors
G. Rouleau
Nature Genetics
1998
Corpus ID: 20485694
Autosomal dominant oculopharyngeal muscular dystrophy (OPMD) is an adult-onset disease with a world-wide distribution1. It…
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Review
1997
Review
1997
Cytochrome c: Can't Live with It—Can't Live without It
John Calvin Reed
Cell
1997
Corpus ID: 19023126
Review
1997
Review
1997
A review of paroxysmal hemicranias, SUNCT syndrome and other short-lasting headaches with autonomic feature, including new cases.
P. Goadsby
,
R. Lipton
Brain : a journal of neurology
1997
Corpus ID: 980335
The short-lasting primary headache syndromes may be conveniently divided into those exhibiting marked autonomic activation and…
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Highly Cited
1997
Highly Cited
1997
Mutations of the TWIST gene in the Saethre-Chotzene syndrome
V. E. Ghouzzi
,
M. Merrer
,
+7 authors
J. Bonaventure
Nature Genetics
1997
Corpus ID: 22140671
Saethre-Chotzen syndrome (acrocephalo-syndactyly type III, ACS III) is an autosomal dominant craniosynostosis with brachydactyly…
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Review
1988
Review
1988
The Lambert-Eaton myasthenic syndrome. A review of 50 cases.
J. H. O'neill
,
N. Murray
,
J. Newsom-Davis
Brain : a journal of neurology
1988
Corpus ID: 5662993
The clinical and electrophysiological features of 50 consecutive patients with the Lambert-Eaton myasthenic syndrome (LEMS) have…
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Highly Cited
1975
Highly Cited
1975
Müller muscle-conjunctiva resection. Technique for treatment of blepharoptosis.
A. Putterman
,
M. Urist
A M A Archives of Ophthalmology
1975
Corpus ID: 13603201
A new technique for resecting the Müller muscle and the conjunctiva for correction of blepharoptosis has been developed. The…
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