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Fechtner syndrome (disorder)
Known as:
APSM, FORMERLY
, MACROTHROMBOCYTOPENIA, NEPHRITIS, DEAFNESS, AND LEUKOCYTE INCLUSIONS
, FTNS
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National Institutes of Health
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Related topics
Related topics
7 relations
Autosomal dominant inheritance
Congenital cataract
Glaucoma of childhood
Hematuria
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2020
Review
2020
Caracterização de fatores predisponentes, sinais e sintomas de disfunção temporomandibular em pacientes das clínicas de prótese dentária da UFCG
Marcos Vinícios da Silva Cavalcante
,
J. H. R. Cruz
,
A. Filho
,
Luanna Abílio Diniz Melquíades de Medeiros
,
Elizandra Silva da Penha
,
Gymenna Maria Tenório Guênes
ARCHIVES OF HEALTH INVESTIGATION
2020
Corpus ID: 219907191
Introdução: Os estudos sobre perda dentária mostram a sua alta prevalência e com isso a necessidade do uso de próteses dentais…
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2020
2020
Fechtner Syndrome
Definitions
2020
Corpus ID: 29612343
An autosomal dominant disorder characterized by the triad of thrombocytopenia, giant platelets, and characteristic inclusions in…
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2016
2016
FASTER THAN NYQUIST SIGNALING BASED ON ENERGY SPREADING TRANSFORM AND IDEAL ENERGY SPREADING TRANSFORM
Geoffrey Y. Li
2016
Corpus ID: 32851221
2011
2011
EUVL alternating phase shift mask
P. Yan
,
A. Myers
,
+4 authors
F. Salmassi
Advanced Lithography
2011
Corpus ID: 123287110
Extreme ultra-violet Lithography (EUVL) alternating phase shift mask (APSM) or other optical enhancement techniques are likely…
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2006
2006
Alternating phase shift mask technology for 65nm logic applications
K. Chakravorty
,
S. Henrichs
,
+12 authors
Jeff N. Farnsworth
SPIE Advanced Lithography
2006
Corpus ID: 109709753
Alternating Phase Shift Mask (APSM) Technology has been developed and successfully implemented for the poly gate of 65nm node…
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2000
2000
Localisation of the gene responsible for Fechtner syndrome in a region <600 Kb on 22q11–q13
Roberto Cusano
,
Simone Gangarossa
,
+6 authors
Marco Seri
European Journal of Human Genetics
2000
Corpus ID: 6256423
Fechtner syndrome is an autosomal dominant disorder which has been thought to be a variant of Alport syndrome. It is…
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2000
2000
Fechtner syndrome: physiologic analysis of macrothrombocytopenia.
R. McBane
,
M. Elliott
,
+4 authors
W. Nichols
Blood Coagulation and Fibrinolysis
2000
Corpus ID: 23490482
Fechtner syndrome is a rare autosomal dominant disorder consisting of macrothrombocytopenia and leukocyte inclusions, associated…
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2000
2000
Das Fechtner-Syndrom Eine seltene Differentialdiagnose des Alport-Syndroms
W. Delb
,
J. Schenk
,
H. Iro
HNO (Berlin. Print)
2000
Corpus ID: 24882216
ZusammenfassungIn dem vorliegenden Artikel wird über eine weitere Familie mit 5 Patienten berichtet, die unter einem Fechtner…
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Review
1998
Review
1998
[Fechtner syndrome].
M. Ohata
Ryōikibetsu shōkōgun shirīzu
1998
Corpus ID: 263382756
Review
1989
Review
1989
[Fechtner syndrome: report of two families and review of the literature on the related disorders].
K. Takai
,
M. Sanada
,
A. Hattori
,
T. Koike
,
A. Shibata
Nihon Ketsueki Gakkai zasshi : journal of Japan…
1989
Corpus ID: 25685924
Two families who had been reported as having May-Hegglin anomaly were diagnosed as having Fechtner syndrome based on complication…
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