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Ernst Hanhart
Observed names:
E HANHART,
E Hanhart,
E. Hanhart,
Hanhart, E.:
Observed institutions:
University of Iowa Hospitals and Clinics,
University Hospital Zurich,
University of Iowa Stead Family Children’s Hospital,
University Children’s Hospital Bern,
University College London
OpenAlex ID:
A5071226012
New special forms of keratosis palmo-plantaris, u. a., a regularly g-dominant with systematized lipomas, furthermore 2 simple-recessive with idiocy and z. T. with corneal changes in the eye (ectodermal syndrome).
1947
·
E HANHART
·
PubMed
·
71
[Familial, juvenile nephronophthisis (idiopathic parenchymal contracted kidney)].
1951
·
G FANCONI
, E HANHART
, et al.
·
PubMed
·
60
Über 27 Sippen mit infantiler amaurotischer Idiotie (Tay-Sachs)
1955
·
E. Hanhart
·
Acta geneticae medicae et gemellologiae
·
26
PDF
Trisomy in Mother and Child
1961
·
E. Hanhart
, JoyD.A. Delhanty
, et al.
·
The Lancet
·
23
Erbpathologie des Stoffwechsels
1940
·
Ernst Hanhart
·
Springer eBooks
·
18
[On heredity in diabetes mellitus].
1951
·
E HANHART
·
PubMed
·
15
The infantile proximal spinal muscular atrophies in Switzerland.
1972
·
H Zellweger
, E Hanhart
·
PubMed
·
8
A new genetic variant of the spinal muscular atrophies in infancy.
1972
·
H Zellweger
, E Hanhart
, et al.
·
Journal of Medical Genetics
·
7
Ueber einfache Rezessivität bei Mikrocephalia vera, spuria et combinata und das herdweise Vorkommen der Mikrocephalia vera in Schweizer Isolaten
1958
·
E. Hanhart
·
Acta geneticae medicae et gemellologiae
·
7
PDF
Eineiige Zwillingsmädchen mit konkordantem Albinismus Universalis aus Ehe normalpigmentierter, aber entsprechend belasteter Vettern I. Grades in oberitalienischem Isolat
1953
·
Ernst Hanhart
·
Acta geneticae medicae et gemellologiae
·
7
PDF
Die Entstehung und Ausbreitung von Mutationen beim Menschen
1940
·
E. Hanhart
·
Springer eBooks
·
7
[The role of hereditary factors in growth disorders].
1953
·
E HANHART
·
PubMed
·
6
Zur Genetischen Abgrenzung Neurologischer Krankheitseinheiten Und Nervöser Belastungen
1963
·
E. Hanhart
·
Acta Psychiatrica Scandinavica
·
5
Die Schweizer Fälle von Splenohepatomegalie (Niemann-Pick) Ein Beitrag zur genetischen Abgrenzung der Phospatid-Lipoidosen
1956
·
E. Hanhart
·
Acta geneticae medicae et gemellologiae
·
5
PDF
Die Rolle der Erbfaktoren bei der Entstehung alimentärer Allergien
2009
·
Ernst Hanhart
·
International Archives of Allergy and Applied Immunology
·
2
About the inheritance of glycogenoses and their relationship to diabetes mellitus.
1947
·
E HANHART
·
PubMed
·
2
[Scientific raisins from 125 years SMW (Swiss Medical Weekly). Contribution to constitutional and hereditary research with the help of studies on hereditary ataxia (46 new cases of Friedreich's disease). 1923].
1995
·
E Hanhart
·
PubMed
·
1
Über die Proximalen Spinalen Muskelatrophien
1972
·
H. Zellweger
, A. Frank
, et al.
·
Neuropediatrics
·
1
[Contribution of genetic factors in suicide based on temporary increase in the rate of familial suicides in Swiss isolates].
1968
·
E Hanhart
·
PubMed
·
1
[I. Genetic correlation of undifferentiated imbecility of all degrees in isolate H].
1967
·
E Hanhart
·
PubMed
·
1
[Present-day aspects of general and human genetics].
1961
·
E HANHART
·
PubMed
·
1
[Dominant heredity of progressive muscular dystrophy in family in Vaud].
1954
·
M JEQUIER
, E HANHART
·
PubMed
·
1
[Genetic aspects of primary myopathies, infantile progressive spinal atrophy (Werdnig-Hoffman atrophy) and neural atrophy (Charcot-Marie-Tooth disease)].
1954
·
E HANHART
·
PubMed
·
1
[Significance of hereditary homo- and heterogeny in hereditary prognosis of clinical signs, especially diabetes mellitus and recessive deafmutism].
1951
·
E HANHART
, R LUCHSINGER
·
PubMed
·
1
On the genetics of some deformities (microtia, peromelia, Pollex varus, hydrocephaly, microcephaly) and on the genesis of so-called amiotic constrictions.
1947
·
E HANHART
·
PubMed
·
1
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Works count:
45
Citation count:
279
H-index:
7
I10-index:
6
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