Die I. Kinderklinik der Medizinischen Semmelweis-Universität zu Budapest―Eine Stätte enger deutsch-ungarischer Verbundenheit―unter dem Gesichtspunkt ihrer medizinhistorischen Schätze = The first department of pediatrics of the semmelweis medical university at Budapest―an area of close German―Hungarian cooperation―with special reference to its historical treasuresWIEDEMANN, H.-R.Klinische Pädiatrie. 1993, Vol 205, Num 1, pp 45-51, issn 0300-8630Article

«Ein schönes Schneiden!» Ein unbekannter Brief Soemmerrings über die Guillotine = An unknown letter of Soemmerring about the guillotineWIEDEMANN, H.-R.Medizinhistorisches Journal. 1992, Vol 27, Num 1-2, pp 126-137, issn 0025-8431Article

Cheek dimplesWIEDEMANN, H.-R.American journal of medical genetics. 1990, Vol 36, Num 3, issn 0148-7299, p.376Article

Genital overgrowth in the EMG syndromeWIEDEMANN, H.-R.American journal of medical genetics. 1989, Vol 32, Num 2, pp 255-256, issn 0148-7299Article

Tumours and hemihypertrophy associated with Wiedemann-Beckwith syndromeWIEDEMANN, H.-R.European journal of pediatrics. 1983, Vol 141, Num 2, issn 0340-6199, 129Article

Salivary gland disorders and heredityWIEDEMANN, H.-R.American journal of medical genetics. 1997, Vol 68, Num 2, pp 222-224, issn 0148-7299Article

Earliest description by Johann Friedrich Meckel, Senior (1750) of what is known today as Lutembacher syndrome (1916)WIEDEMANN, H.-R.American journal of medical genetics. 1994, Vol 53, Num 1, pp 59-64, issn 0148-7299Article

Historical case of dwarfism : attempted diagnosisWIEDEMANN, H.-R.American journal of medical genetics. 1993, Vol 47, Num 5, pp 805-806, issn 0148-7299Article

LADD syndrome: report of new cases and review of the clinical spectrumWIEDEMANN, H.-R; DRESCHER, J.European journal of pediatrics. 1986, Vol 144, Num 6, pp 579-582, issn 0340-6199Article

Metaphyseal anadysplasia: observation of a patient from infancy to the fifth decade of lifeWIEDEMANN, H.-R.Dysmorphology and clinical genetics. 1992, Vol 6, Num 3, pp 123-127, issn 0893-6633Conference Paper

Stüve-Wiedemann syndrome : Update and historical footnoteWIEDEMANN, H.-R; STÜVE, A.American journal of medical genetics. 1996, Vol 63, Num 1, pp 12-16, issn 0148-7299Article

Chondrodysplasia punctata in an adult recognized as vitamin K antagonist embryopathyHOSENFELD, D; WIEDEMANN, H.-R.Clinical genetics. 1989, Vol 35, Num 5, pp 376-381, issn 0009-9163, 6 p.Article

Unusual complex of ventral midline anomalies : A multiple congenital anomalies/mental retardation syndromeBOHRING, A; SONNTAG, J; SCHRÖDER, H et al.American journal of medical genetics. 1996, Vol 66, Num 4, pp 453-456, issn 0148-7299Article

Neonatales progeroides Syndrom (Wiedemann-Rautenstrauch): eine follow-up-Studie = Neonatal progeroid syndrome (Widemann-Rautenstrauch): a follow-up studyRAUTENSTRAUCH, T; SNIGULA, F; WIEDEMANN, H.-R et al.Klinische Pädiatrie. 1994, Vol 206, Num 6, pp 440-443, issn 0300-8630Article

Hirsutism-skeletal dysplasia-mental retardation syndrome with abnormal face and a uric acid metabolism disorderWIEDEMANN, H.-R; OLDIGS, H.-D; OPPERMANN, H.-C et al.American journal of medical genetics. 1993, Vol 46, Num 4, pp 403-409, issn 0148-7299Article

Previously unrecognized congenital progeroid disorderPETTY, E. M; LAXOVA, R; WIEDEMANN, H.-R et al.American journal of medical genetics. 1990, Vol 35, Num 3, pp 383-387, issn 0148-7299Article

Polytopic anomalies with agenesis of the lower vertebral columnBOHRING, A; LEWIN, S. O; GRITTER, H. L et al.American journal of medical genetics. 1999, Vol 87, Num 2, pp 99-114, issn 0148-7299Article

Robin sequence and oligodactyly in mother and son ― probably a further example of the postaxial acrofacial dysostosis syndrome. ReplyMEINECKE, P; WIEDEMANN, H.-R; ROBINOW, M et al.American journal of medical genetics. 1987, Vol 27, Num 4, pp 953-957, issn 0148-7299Article

Prenatal diagnosis of a probable hereditary syndrome with holoprosencephaly, hydrocephaly, octodactyly, and cardiac malformationsGROTE, W; REHDER, H; WEISNER, D et al.European journal of pediatrics. 1984, Vol 143, Num 2, pp 155-157, issn 0340-6199Article

Pterygium colli medianum and midline cervical cleft: midline anomalies in the sense of a developmental field defect (brief clinical report)GODBERSEN, S; HECKEL, V; WIEDEMANN, H.-R et al.American journal of medical genetics. 1987, Vol 27, Num 3, pp 719-723, issn 0148-7299Article

Probable autosomal recessive syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal earSCHLEGELBERGER, B; GROTE, W; WIEDEMANN, H.-R et al.Klinische Pädiatrie. 1986, Vol 198, Num 4, pp 337-339, issn 0300-8630Article

Further and new details on the proteus syndromeBURGIO, G. R; WIEDEMANN, H.-R.European journal of pediatrics. 1984, Vol 143, Num 1, pp 71-73, issn 0340-6199Article

Blepharo-Cheilo-Dontic (BCD) syndromeGORLIN, R. J; ZELLWEGER, H; CURTIS, M. W et al.American journal of medical genetics. 1996, Vol 65, Num 2, pp 109-112, issn 0148-7299Article

Proteus syndrome : course of a severe caseMALAMITSI-PUCHNER, A; DIMITRIADIS, D; BARTSOCAS, C et al.American journal of medical genetics. 1990, Vol 35, Num 2, pp 283-285, issn 0148-7299Article

Growth, bone maturation and pubertal development in children with the EMG-syndromeSIPPELL, W. G; PARTSCH, C.-J; WIEDEMANN, H. R et al.Clinical genetics. 1989, Vol 35, Num 1, pp 20-28, issn 0009-9163Article