UB Paderborn / Katalog / Suche / in CDI

Maternal and infantile protection in Poland

Revue médicale de Liège, 1966-05, Vol.21 (10), p.237

Goncerzewicz, M

1966

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Study of the metabolism of an enzymatic system in phenylketonuria

Revue médicale de Liège, 1966-01, Vol.21 (1), p.1

Goncerzewicz, M

1966

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Vitamin-D-Stoffwechsel bei Kindern mit Malabsorptionssyndrom

Klinische Pädiatrie, 1985, Vol.197 (1), p.30-34

1985

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Studies on the enzymatic and genetic system in phenylalanine metabolism disorders

Pediatria polska, 1962-11, Vol.37, p.1173-1178

GONCERZEWICZ, M

1962

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Simple methods for the diagnosis of phenylalaninuria

Polski tygodnik lekarski (Warsaw, Poland : 1960), 1962-08, Vol.17, p.1270

GONCERZEWICZ, M

1962

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Medical program of the Memorial Hospital of the Child Health Center

Pediatria polska, 1987-02, Vol.62 (2), p.73-75

Goncerzewicz, M

1987

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Pancreatitis in children and adolescents

Materia medica Polona. Polish journal of medicine and pharmacy, 1986-04, Vol.18 (2), p.94

1986

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Activity of jejunal peptidases in malabsorption syndrome in children (author's transl)

Przeglad lekarski, 1979, Vol.36 (2), p.259

1979

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Oleandomycin-tetracycline in the treatment of infections in children: in vivo and in vitro studies

International record of medicine, 1961-05, Vol.174, p.307

1961

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Spiramycin in the treatment of infections in children: in vivo and in vitro studies

International record of medicine, 1961-02, Vol.174, p.80

1961

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Psychosomatic development of children with malabsorption syndrome

Pediatria polska, 1975-10, Vol.50 (10), p.1201-1211

1975

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Memorial Hospital of the Children's Health Center

Pediatria polska, 1979-06, Vol.54 (6), p.593-598

Goncerzewicz, M

1979

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Our observations on genetic prophylaxis in phenylketonuria

Pediatria polska, 1965-06, Vol.40 (6), p.601-604

Goncerzewicz, M

1965

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CONTRIBUTION TO THE STUDY OF MENTAL DEFICIENCY ETIOLOGY IN CASES OF INBORN ERRORS OF PHENYLALANINE METABOLISM

Pediatria polska, 1965-03, Vol.40, p.259-260

GONCERZEWICZ, M

1965

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OUR OBSERVATIONS ON THE PROBLEM OF THE TREATMENT OF PHENYLKETONURIA

Pediatria polska, 1963-01, Vol.38, p.33-41

GONCERZEWICZ, M

1963

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Determination of C-reactive proteins as a supplementary method of investigation of inflammatory processes in children

Pediatria polska, 1959-02, Vol.34 (2), p.131-144

GONCERZEWICZ, M

1959

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Vitamin D metabolism in children with malabsorption syndrome

Klinische Pädiatrie, 1985-01, Vol.197 (1), p.30-34

1985

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Family environment and health status of mentally retarded children

Pediatria polska, 1980-10, Vol.55 (10), p.1101-1110

1980

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Unusual case of congenital absence of the spleen and congenital cardiovascular defects with complete intestinal situs inversus

Polski tygodnik lekarski, 1957-11, Vol.12 (46), p.1785

GONCERZEWICZ, M

1957

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Postprandial gastrinemia and insulinemia in children with malabsorption syndromes

Pediatria polska, 1978-08, Vol.53 (8), p.925-931

1978

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Problems of sports in children and adolescents from the standpoint of a pediatrician

Pediatria polska, 1972-12, Vol.47 (12), p.1541-1548

1972

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Assessment of nutritional state in children with untreated phenylketonuria

Pediatria polska, 1973-05, Vol.48 (5), p.567-574

1973

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Developmental control clinics

Pediatria polska, 1970-12, Vol.45 (12), p.1529-1536

1970

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Treatment of stuttering in children with prolonged sleep

Pediatria polska, 1956-03, Vol.31 (3), p.317-323

1956

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Food stimulated release of IRI and HGH in children with malabsorption (author's transl)

Monatsschrift Kinderheilkunde, 1980-12, Vol.128 (12), p.770-772

1980

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Maternal and infantile protection in Poland

Study of the metabolism of an enzymatic system in phenylketonuria

Vitamin-D-Stoffwechsel bei Kindern mit Malabsorptionssyndrom

Studies on the enzymatic and genetic system in phenylalanine metabolism disorders

Simple methods for the diagnosis of phenylalaninuria

Medical program of the Memorial Hospital of the Child Health Center

Pancreatitis in children and adolescents

Activity of jejunal peptidases in malabsorption syndrome in children (author's transl)

Oleandomycin-tetracycline in the treatment of infections in children: in vivo and in vitro studies

Spiramycin in the treatment of infections in children: in vivo and in vitro studies

Psychosomatic development of children with malabsorption syndrome

Memorial Hospital of the Children's Health Center

Our observations on genetic prophylaxis in phenylketonuria

CONTRIBUTION TO THE STUDY OF MENTAL DEFICIENCY ETIOLOGY IN CASES OF INBORN ERRORS OF PHENYLALANINE METABOLISM

OUR OBSERVATIONS ON THE PROBLEM OF THE TREATMENT OF PHENYLKETONURIA

Determination of C-reactive proteins as a supplementary method of investigation of inflammatory processes in children

Vitamin D metabolism in children with malabsorption syndrome

Family environment and health status of mentally retarded children

Unusual case of congenital absence of the spleen and congenital cardiovascular defects with complete intestinal situs inversus

Postprandial gastrinemia and insulinemia in children with malabsorption syndromes

Problems of sports in children and adolescents from the standpoint of a pediatrician

Assessment of nutritional state in children with untreated phenylketonuria

Developmental control clinics

Treatment of stuttering in children with prolonged sleep

Food stimulated release of IRI and HGH in children with malabsorption (author's transl)

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