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Results: 1-25/31
Authors:
JANSSEN G
MESSINGJUNGER AM
ENGELBRECHT V
GOBEL U
BOCK WJ
LENARD HG
Citation: G. Janssen et al., CEREBELLAR MUTISM SYNDROME, Klinische Padiatrie, 210(4), 1998, pp. 243-247
Authors:
ROSENBAUM T
GARTNER J
KORHOLZ D
JANSSEN G
SCHNEIDER D
ENGELBRECHT V
GOBEL U
LENARD HG
Citation: T. Rosenbaum et al., PARANEOPLASTIC LIMBIC ENCEPHALITIS IN 2 TEENAGE GIRLS, Neuropediatrics, 29(3), 1998, pp. 159-162
Authors:
CALAMINUS G
JANSSEN G
LENARD HG
BOCK WJ
REIFENBERGER G
SCHMITT G
GOBEL U
Citation: G. Calaminus et al., COMBINED THERAPY OF MEDULLOBLASTOMA - REVIEW OF 46 PATIENTS TREATED IN A SINGLE INSTITUTION, Neuropediatrics, 29(2), 1998, pp. 102-107
Authors:
GARTNER J
BRAUN A
HOLZINGER A
ROERIG P
LENARD HG
ROSCHER AA
Citation: J. Gartner et al., CLINICAL AND GENETIC-ASPECTS OF X-LINKED ADRENOLEUKODYSTROPHY, Neuropediatrics, 29(1), 1998, pp. 3-13
Authors:
GOHLICHRATMANN G
BAETHMANN M
LORENZ P
GARTNER J
GOEBEL HH
ENGELBRECHT V
CHRISTEN HJ
LENARD HG
VOIT T
Citation: G. Gohlichratmann et al., MEGALENCEPHALY, MEGA CORPUS-CALLOSUM, AND COMPLETE LACK OF MOTOR DEVELOPMENT - A PREVIOUSLY UNDESCRIBED SYNDROME, American journal of medical genetics, 79(3), 1998, pp. 161-167
Authors:
HORNEFF G
JOCHUM F
SCHROTEN H
LENARD HG
Citation: G. Horneff et al., ERYTHROMELALGIA IN A CHILD - SUCCESSFUL TREATMENT WITH SODIUM-NITROPRUSSIDE, Monatsschrift fur Kinderheilkunde, 146(9), 1998, pp. 865-867
Authors:
REIFENBERGER J
JANSSEN G
WEBER RG
BOSTROM J
ENGELBRECHT V
LICHTER P
BORCHARD F
GOBEL U
LENARD HG
REIFENBERGER G
Citation: J. Reifenberger et al., PRIMITIVE NEUROECTODERMAL TUMORS OF THE CEREBRAL HEMISPHERES IN 2 SIBLINGS WITH TP53 GERMLINE MUTATION, Journal of neuropathology and experimental neurology, 57(2), 1998, pp. 179-187
Authors:
HOFMANN B
SCHUPPE HC
ADAMS O
LENARD HG
LEHMANN P
RUZICKA T
Citation: B. Hofmann et al., GIANOTTI-CROSTI-SYNDROME ASSOCIATED WITH EPSTEIN-BARR-VIRUS INFECTION, Pediatric dermatology, 14(4), 1997, pp. 273-277
Authors:
PREIS S
SCHITTLER P
LENARD HG
Citation: S. Preis et al., MOTOR-PERFORMANCE AND HANDEDNESS IN CHILDREN WITH DEVELOPMENTAL LANGUAGE DISORDER, Neuropediatrics, 28(6), 1997, pp. 324-327
Authors:
PREIS S
SCHITTLER P
RICHTERWERKLE R
STERZEL U
LENARD HG
Citation: S. Preis et al., TYPICAL PATTERN OF THE KAUFMAN-ASSESSMENT BATTERY IN CHILDREN WITH DEVELOPMENTAL LANGUAGE DISORDER, Neuropediatrics, 28(6), 1997, pp. 328-332
Authors:
SCHURMANN M
ENGELBRECHT V
LOHMEIER K
LENARD HG
WENDEL U
GARTNER J
Citation: M. Schurmann et al., CEREBRAL METABOLIC CHANGES IN BIOTINIDASE DEFICIENCY, Journal of inherited metabolic disease, 20(6), 1997, pp. 755-760
Authors:
KELLER KM
NOEKER M
HILLIGES C
LENARD HG
LENTZE MJ
Citation: Km. Keller et al., CHILD-ABUSE PRESENTING AS MUNCHAUSEN-BY-P ROXY SYNDROME, Monatsschrift fur Kinderheilkunde, 145(11), 1997, pp. 1156-1162
Authors:
BAETHMANN M
KAHN T
LENARD HG
VOIT T
Citation: M. Baethmann et al., FETAL CNS DAMAGE AFTER EXPOSURE TO MATERNAL TRAUMA DURING PREGNANCY, Acta paediatrica, 85(11), 1996, pp. 1331-1338
Authors:
PREIS S
MAJEWSKI F
HANTSCHMANN R
SCHUMACHER H
LENARD HG
Citation: S. Preis et al., GOLDENHAR, MOBIUS AND HYPOGLOSSIA-HYPODACTYLY ANOMALIES IN A SYNDROMEOR ASSOCIATION, European journal of pediatrics, 155(5), 1996, pp. 385-389
Authors:
COHN RD
GILLESSENKAESBACH G
DOBYNS WB
KAHN T
LENARD HG
VOIT T
Citation: Rd. Cohn et al., DIFFUSE POLYMICROGYRIA ASSOCIATED WITH AN UNUSUAL PATTERN OF MULTIPLECONGENITAL-ANOMALIES INCLUDING TURRIBRACHYCEPHALY AND HYPOGENITALISM, American journal of medical genetics, 63(1), 1996, pp. 314-317
Authors:
DIERKS C
BAUMANN TG
LENARD HG
Citation: C. Dierks et al., RECOMMENDATIONS ON DENIAL OF THERAPY FOR CHILDREN AND ADOLESCENTS, Monatsschrift fur Kinderheilkunde, 144(8), 1996, pp. 843-844
Authors:
PREIS S
ENGELBRECHT V
LENARD HG
Citation: S. Preis et al., APLASIA-CUTIS-CONGENITA AND ENLARGED PARIETAL FORAMINA (CATLIN MARKS)IN A FAMILY, Acta paediatrica, 84(6), 1995, pp. 701-702
Authors:
LENARD HG
Citation: Hg. Lenard, ETHICAL PROBLEMS IN PRENATAL-DIAGNOSIS - PEDIATRIC CONSIDERATIONS, Brain & development, 17, 1995, pp. 44-47
Authors:
VOIT T
SEWRY CA
MEYER K
HERMANN R
STRAUB V
MUNTONI F
KAHN T
UNSOLD R
HELLIWELL TR
APPLETON R
LENARD HG
Citation: T. Voit et al., PRESERVED MEROSIN M-CHAIN (OR LAMININ-ALPHA(2)) EXPRESSION IN SKELETAL-MUSCLE DISTINGUISHES WALKER-WARBURG SYNDROME FROM FUKUYAMA MUSCULAR-DYSTROPHY AND MEROSIN-DEFICIENT CONGENITAL MUSCULAR-DYSTROPHY, Neuropediatrics, 26(3), 1995, pp. 148-155
Authors:
BARTH PG
BLENNOW G
LENARD HG
BEGEER JH
VANDERKLEY JM
HANEFELD F
PETERS ACB
VALK J
Citation: Pg. Barth et al., THE SYNDROME OF AUTOSOMAL RECESSIVE PONTOCEREBELLAR HYPOPLASIA, MICROCEPHALY, AND EXTRAPYRAMIDAL DYSKINESIA (PONTOCEREBELLAR HYPOPLASIA TYPE-2) - COMPILED DATA FROM 10 PEDIGREES, Neurology, 45(2), 1995, pp. 311-317
Authors:
ECKHOFDONOVAN S
SCHWARZ TF
BAETHMANN M
VOIT T
LENARD HG
Citation: S. Eckhofdonovan et al., PAPPATACI-FEVER AS DIFFERENTIAL-DIAGNOSIS OF MENINGITIS IN CHILDHOOD, Monatsschrift fur Kinderheilkunde, 143(9), 1995, pp. 839-842
Authors:
PREIS S
MAJEWSKI F
KUSTER WJK
LENARD HG
Citation: S. Preis et al., CONGENITAL SKIN-LESIONS - SYMPTOM OF HETE ROGENEOUS CLINICAL CASES, Monatsschrift fur Kinderheilkunde, 143(4), 1995, pp. 334-340
Authors:
LENARD HG
Citation: Hg. Lenard, OBSERVATIONS ON THE ETHICS OF PRENATAL-DI AGNOSIS ACCORDING TO THE PEDIATRICIAN, Der Gynakologe, 28(5), 1995, pp. 384-388
Authors:
WESSALOWSKI R
SCHROTEN H
NEUENJACOB E
REICHMANN H
MELNIK BC
LENARD HG
VOIT T
Citation: R. Wessalowski et al., MULTISYSTEM TRIGLYCERIDE STORAGE DISORDER WITHOUT ICHTHYOSIS IN 2 SIBLINGS, Acta paediatrica, 83(1), 1994, pp. 93-98
Authors:
PENNINGS CM
SEITZ RC
KARCH H
LENARD HG
Citation: Cm. Pennings et al., HEMOLYTIC-ANEMIA IN ASSOCIATION WITH ESCHERICHIA-COLI-O157 INFECTION IN 2 SISTERS, European journal of pediatrics, 153(9), 1994, pp. 656-658