G. Neuhäuser

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Studies of malformation syndromes of man XXXVIII: the BD syndrome

J. Opitz, G. Neuhäuser, E. Kaveggia, 1975, Zeitschrift für Kinderheilkunde.

Analysis of etiologic factors in cerebral palsy with severe mental retardation

J. Opitz, G. Neuhäuser, E. Kaveggia, 1976, European Journal of Pediatrics.

Benign hereditary non-progressive chorea of early onset. Clinical genetics of the syndrome and report of a new family.

L. Tomasi, G. Neuhäuser, J. Burns, 1976, Neuropadiatrie.

Studies of malformation syndromes in man XXXX: Multiple congenital anomalies/mental retardation syndrome or variant familial developmental pattern; differential diagnosis and description of the McDonough syndrome (with XXY son from XY/XXY father)

J. Opitz, G. Neuhäuser, 1975, Zeitschrift für Kinderheilkunde.

Development of Infants “At Risk” and Psychosocial Conditions: Results of a Prospective Study

G. Neuhäuser, 1989 .

Congenital intracranial neoplasms

I. Ellams, A. Agnoli, G. Neuhäuser, 2004, Child's Nervous System.

CYTOPLASMIC INCLUSIONS IN A CHILD AFFECTED WITH KRABBE'S DISEASE (GLOBOID LEUCODYSTROPHY) AND IN THE RABBIT INJECTED WITH GALACTOCEREBROSIDES

G. Neuhäuser, A. Anzil, K. Blinzinger, 1972, Journal of neuropathology and experimental neurology.

Studies of malformation syndromes of man XXXIX: A craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: “Craniofacial dyssynostosis”

J. Opitz, G. Neuhäuser, E. Kaveggia, 1976, European Journal of Pediatrics.

Minor craniofacial anomalies in children

G. Neuhäuser, J. Vogl, 1980, European Journal of Pediatrics.

[Clinical picture of encephalitis in children].

G. Neuhäuser, A. Windorfer, 1973, Deutsche medizinische Wochenschrift.

Fatal CNS dysgenesis with severe microencephaly, mental retardation, seizures and paucity of myelin, autosomal recessive trait?

J. Opitz, G. ZuRhein, G. Neuhäuser, 1977, European Journal of Pediatrics.

Autosomal recessive syndrome of cerebellar ataxia and hypogonadotropic hypogonadism *

J. Opitz, G. Neuhäuser, J. M. Opitz, 1975, Clinical genetics.

Syndrome of mental retardation, seizures, hypotonic cerebral palsy and megalocorneae, recessively inherited

J. Opitz, T. France, G. Neuhäuser, 1975, Zeitschrift für Kinderheilkunde.

Familial spastic paraplegia with distal muscle wasting in the Old Order Amish; atypical Troyer syndrome or “new” syndrome *

J. Opitz, G. Neuhäuser, C. Wiffler, 1976, Clinical genetics.

CNS late effects after ALL therapy in childhood. Part II: Conventional EEG recordings in asymptomatic long-term survivors of childhood ALL--an evaluation of the interferences between neurophysiology, neurology, psychology, and CNS morphology. German Late Effects Working Group.

W. Huk, F. Lampert, R. Korinthenberg, 1997, Medical and pediatric oncology.

[G-deletion syndrome].

G. Neuhäuser, 1973, Hippokrates.

Growth variables and brain damage at birth predict developmental disability at four years of age : A basis for individual preschool support 1

A. Jensen, G. Neuhäuser, Kai-Ole Jensen, 2019 .

EEG in childhood epilepsy : initial presentation and long-term follow-up

H. Doose, B. Neubauer, G. Neuhäuser, 2003 .

X‐linked congenital ataxia: A new locus maps to Xq25‐q27.1

J. Opitz, E. Bertini, J. Chelly, 2008, American journal of medical genetics. Part A.

[Abnormalities of the central nervous system in the area of the posterior cranial fossa--neuroradiologic and clinical aspects].

A. Agnoli, G. Neuhäuser, B. Lochner, 1986, Klinische Padiatrie.

Heterogeneity of X-linked recessive (spino)cerebellar ataxia with or without spastic diplegia.

F. Darendeliler, N. Saka, M. Ozmen, 1989, American journal of medical genetics.

[The kinky-hair syndrome of Menkes (author's transl)].

A. Kielhorn, G. Neuhäuser, D. Heye, 1973, Klinische Padiatrie.

Cranial computerized tomography in children with lymphoid malignancy and seizures

W. Huk, G. Neuhäuser, H. Schwenk, 1978, European Journal of Pediatrics.

Mac Keith Meetings

T. Kakebeeke, G. Neuhäuser, Mac Keith Meetings, 2001 .

"ADAM complex" (amniotic deformity, adhesions, mutilations)--a pattern of craniofacial and limb defects.

F. Sitzmann, G. Neuhäuser, E. Kaveggia, 1978, American journal of medical genetics.