Volume 141, Issue 3

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January 1984

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17 articles in this issue

The pioneers of pediatric medicine

Announcement Pages: 133 - 133
Oncogenes: Clues to carcinogenesis
C. R. Bartram
Reviews Pages: 134 - 142
The cephalosporin compounds in severe neonatal infection
Urs B. Schaad
Reviews Pages: 143 - 146
The tay syndrome (congenital ichthyosis with trichothiodystrophy)
R. Happle
H. Traupe
G. Bonsmann
Original Investigations Pages: 147 - 152
Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid
C. Jakobs
L. Sweetman
W. L. Nyhan
Original Investigations Pages: 153 - 157
Parathyroid function in different stages of vitamin D deficiency rickets
K. Kruse
H. Bartels
Ute Kracht
Original Investigations Pages: 158 - 162
Limited joint mobility and diabetic retinopathy demonstrated by fluorescein angiography
A. L. Rosenbloom
J. I. Malone
T. C. Van Cader
Original Investigations Pages: 163 - 164
Generalized lymphadenitis following B.C.G. vaccination in an immunocompetent 12-year-old boy
Z. Katzir
E. Okon
H. Haas
Original Investigations Pages: 165 - 167
Pulsatile secretion of luteinizing hormone and sleep-related gonadotropin rhythms in girls with premature thelarche
W. Beck
P. Stubbe
Original Investigations Pages: 168 - 170
Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival
W. E. Winter
J. H. Silverstein
E. Kiel
Case Reports Pages: 171 - 172
Unusual progression of a Legionella pneumophila infection in a young child
P. Beyer
D. Kahn
B. Weber
Case Reports Pages: 173 - 175
Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13)
J. L. Bernard
M. A. Baeteman
F. Giraud
Case Reports Pages: 175 - 177
Deficiency of cytochromes b and aa₃ in muscle from a floppy infant with cytochrome oxidase deficiency
R. C. A. Sengers
J. M. F. Trijbels
H. J. ter Laak
Case Reports Pages: 178 - 180
Thyroid hormone unresponsiveness in two siblings with intrauterine growth retardation and exophthalmos
Takehiko Ohzeki
Shinzo Egi
Kei Hachimori
Case Reports Pages: 181 - 183
Opitz trigonocephaly syndrome: Report of two cases
S. D. Flatz
A. Schinzel
E. Eilers
Case Reports Pages: 183 - 185
Sodium nitroprusside treatment in erythromelalgia
S. Özsoylu
T. Coskun
Case Reports Pages: 185 - 187
Fetal head growth retardation associated with maternal phenobarbitone/primidone and/or phenytoin therapy
F. Majewski
M. Steger
Letter to the Editors Pages: 188 - 189

Volume 141, Issue 3

The pioneers of pediatric medicine

Oncogenes: Clues to carcinogenesis

The cephalosporin compounds in severe neonatal infection

The tay syndrome (congenital ichthyosis with trichothiodystrophy)

Prenatal diagnosis of glutaric aciduria type II by direct chemical analysis of dicarboxylic acids in amniotic fluid

Parathyroid function in different stages of vitamin D deficiency rickets

Limited joint mobility and diabetic retinopathy demonstrated by fluorescein angiography

Generalized lymphadenitis following B.C.G. vaccination in an immunocompetent 12-year-old boy

Pulsatile secretion of luteinizing hormone and sleep-related gonadotropin rhythms in girls with premature thelarche

Familial DiGeorge syndrome with tetralogy of Fallot and prolonged survival

Unusual progression of a Legionella pneumophila infection in a young child

Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13)

Deficiency of cytochromes b and aa₃ in muscle from a floppy infant with cytochrome oxidase deficiency

Thyroid hormone unresponsiveness in two siblings with intrauterine growth retardation and exophthalmos

Opitz trigonocephaly syndrome: Report of two cases

Sodium nitroprusside treatment in erythromelalgia

Fetal head growth retardation associated with maternal phenobarbitone/primidone and/or phenytoin therapy

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