H. Bickel

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Determination of Phenylalanine Hydroxylase Activity in Patients with Phenylketonuria and Hyperphenylalaninemia

P. Lutz, K. Bartholomé, H. Bickel, 1975, Pediatric Research.

Genotype-phenotype correlations in phenylketonuria.

P. Burgard, U. Lichter-Konecki, D. Konecki, 1993, Clinica chimica acta; international journal of clinical chemistry.

Inborn Errors of Calcium and Bone Metabolism

H. Bickel, J. Stern, 1976 .

[THE "BLUE DIAPER" SYNDROME].

H. Bickel, 1965, Deutsche medizinische Wochenschrift.

[Pulmonary function in bronchial carcinoma].

H. Bickel, 1959, Schweizerische medizinische Wochenschrift.

Growth and skeletal maturation in children with phenylketonuria

A. Rupp, H. Bremer, P. Burgard, 1994, Acta paediatrica.

SOME BIOCHEMICAL ASPECTS OF LIGNAC‐FANCONI DISEASE

H. Bickel, E. M. Hickmans, 1952 .

Mellituria, a paper chromatographic study.

H. Bickel, 1961, The Journal of pediatrics.

Cystine Storage Disease with Aminoaciduria and Dwarfism (LIGNAC—FANCONI DISEASE): INTRODUCTION

J. Smellie, H. Bickel, E. M. Hickmans, 1952 .

Cystine Storage Disease with Aminoaciduria and Dwarfism (Lignac‐Fanconi Disease)

H. Bickel, 1953, Acta paediatrica.

CLINICAL DESCRIPTION, FACTUAL ANALYSIS, PROGNOSIS AND TREATMENT OF LIGNAC‐FANCONI DISEASE

J. Smellie, H. Bickel, E. M. Hickmans, 1952 .

MORBID ANATOMY, HISTOLOGY AND PATHOGENESIS OF LIGNAC‐FANCONI DISEASE: (Cystine Storage Disease with Aminoaciduria)

H. Bickel, H. Baar, 1952 .

Ornithine-ketoacid aminotransferase in human liver with reference to patients with hyperornithinaemia and familial protein intolerance.

N. Räihä, H. Bickel, M. Kekomäki, 1969, Clinica chimica acta; international journal of clinical chemistry.

Influence of phenylalanine intake on phenylketonuria.

H. Bickel, J. Gerrard, E. M. Hickmans, 1953, Lancet.

The Influence of Phenylalanine Intake on the Chemistry and Behaviour of a Phenylketonuric Child

H. Bickel, E. M. Hickmans, J. Gerhard, 2001 .

The Influence of Phenylalanine Intake on the Chemistry and Behaviour of a Phenylketonuria Child

J. Gerrard, H. Bickel, E. M. Hickmans, 1954, Acta paediatrica.

Effect of stopping low-phenylalanine diet on intellectual progress of children with phenylketonuria.

H. Schmidt, O. Wolff, H. Bickel, 1978, Annals of clinical biochemistry.

Rationale of Neonatal Screening for Inborn Errors of Metabolism

H. Bickel, 1980 .

Metabolic disorders in the aetiology of mental retardation

H. Bickel, 1984 .

Neonatal mass screening for metabolic disorders

O. Giardini, C. Bachmann, G. Hammersen, 1981, European Journal of Pediatrics.

Detection of some new abnormal metabolites in the urine of phenylketonuria.

H. Bickel, R. J. Boscott, 1953, Scandinavian journal of clinical and laboratory investigation.

Requirement and Utilization of Carbohydrates and Alcohol

M. Halmágyi, H. Bickel, 1976 .

Significance of the in vivo deuterated phenylalanine load for long-term phenylalanine tolerance and psychointellectual outcome in patients with PKU

F. Trefz, H. Schmidt, H. Bickel, 2005, European Journal of Pediatrics.

PKU and NON‐PKU Hyperphenylalaninemia: Differentiation, Indication for Therapy and Therapeutic Results

U. Lichter-Konecki, D. Konecki, F. Trefz, 1988, Acta paediatrica Japonica : Overseas edition.

Dietary treatment of inborn errors of amino acid and carbohydrate metabolism.

H. Schmidt, H. Bickel, L. Schürrle, 1973, Bibliotheca nutritio et dieta.

Incorporation of shikimate and other precursors into aromatic amino acids and prenylquinones of isolated spinach chloroplasts

G. Schultz, H. Bickel, Lotte Palme, 1978 .

[Functional defects of the proximal tubule].

H. Bickel, 1961, Schweizerische medizinische Wochenschrift.

Inter-laboratory quality control in neonatal screening for inborn errors of metabolism

D. Mathias, H. Bickel, 1985, European Journal of Pediatrics.

Phenylalanine levels in PKU following minor surgery.

S. Cederbaum, M. Miller, H. Bickel, 1982, American journal of medical genetics.

[Evaluation of the dietary treatment of cystinosis].

P. Lutz, H. Schmidt, H. Bickel, 1973, Monatsschrift fur Kinderheilkunde.

Phenylalanine and tyrosine metabolism in patients with phenylketonuria.

H. Bickel, R. J. Boscott, 1953, The Biochemical journal.

Neonatal Screening for Inborn Errors of Metabolism

G. Hammersen, R. Guthrie, H. Bickel, 1980, Springer Berlin Heidelberg.

Cystine storage disease with amino-aciduria.

J. Smellie, H. Bickel, 1952, Lancet.

On the intracellular site of biosynthesis of α-tocopherol in Hordeum vulgare

G. Schultz, H. Bickel, Yvonne Huchzermeyer, 1976 .

Biosynthesis of plastoquinone and β-carotene in isolated chloroplasts

G. Schultz, H. Bickel, 1976 .

Oligosaccharides in infants' faeces

S. Baar, H. Bickel, 1964, Journal of clinical pathology.

Phenylketonuria: Past, present, future

H. Bickel, 1980, Journal of Inherited Metabolic Disease.

[Exchange transfusion as a prophylactic measure in kernicterus in premature infants].

H. Bickel, F. Linneweh, 1957, Klinische Wochenschrift.

Hyperamino-aciduria in Lignac-Fanconi Disease, in Galactosaemia and in an Obscure Syndrome

H. Bickel, D. Thursby-Pelham, 1954, Archives of disease in childhood.

Shikimate pathway regulation in suspensions of intact spinach chloroplasts

G. Schultz, H. Bickel, 1979 .

[On iron-containing growth factors, sideramines, and their antagonists, the iron-containing antibiotics, sideromycins].

V. Prelog, E. Vischer, W. Keller-Schierlein, 1960, Experientia.

Constitution of ferrimycin A1.

V. Prelog, H. Bickel, J. Seibl, 1965, Antimicrobial agents and chemotherapy.

Recent advances in the early detection and treatment of inborn errors with brain damage.

H. Bickel, 1969, Neuropadiatrie.

Maple syrup urine disease: Treatment of the acutely ill newborn

P. Lutz, G. Hammersen, H. Schmidt, 1978, European Journal of Pediatrics.

Tyrosinose@@@Tyrosinosis: Primre und sekundre biochemische Vernderungen@@@Primary and secondary metabolic disturbances

P. Lutz, H. Bickel, W. Ntzenadel, 1972 .

Synthetic Diets in the Treatment of Inborn Errors of Metabolism

H. Schmidt, H. Bickel, L. Schürrle, 1973 .

The introduction of newborn screening for phenylketonuria

R. Guthrie, H. Bickel, 2009, European Journal of Pediatrics.

Follow-up study of 16 years neonatal screening for inborn errors of metabolism in West Germany

D. Mathias, H. Bickel, 1986, European Journal of Pediatrics.

Recommendations for Newborn Screening

J. Colombo, G. Hammersen, H. Bickel, 1980 .

The first treatment of phenylketonuria

H. Bickel, 2009, European Journal of Pediatrics.

Phenylketonuria and some other inborn errors of amino acid metabolism : biochemistry, genetics, diagnosis, therapy

F. Hudson, L. Woolf, H. Bickel, 1971 .

A clinical and biochemical study of hepatolenticular degeneration (Wilson's disease).

H. Bickel, F. C. Neale, G. Hall, 1957, The Quarterly journal of medicine.

[Development of biochemical lesions in the Lignac-Fanconi syndrome].

H. Bickel, 1955, Helvetica paediatrica acta.

[Maple syrup urine disease with an intermittent relatively benign course].

P. Lutz, H. Bickel, H. Müller, 1971, Deutsche medizinische Wochenschrift.

Phenylalaninaemia or classical phenylketonuria (PKU)?

H. Bickel, 1970, Neuropadiatrie.

[Phenylketonuria. Psychometric assessment of the phenylalanine-poor diet in children with phenylketonuria].

H. Bickel, S. Kaiser-Grubel, 1971, Deutsche medizinische Wochenschrift.

[Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease].

G. Fanconi, H. Bickel, 1949, Helvetica paediatrica acta.

Neuropsychological and biochemical investigations in heterozygotes for phenylketonuria during ingestion of high dose aspartame (a sweetener containing phenylalanine)

L. Sonneville, P. Matthis, C. Benninger, 1994, Human Genetics.

Hereditary tubular disorders of the Fanconi type and the idiopathic Fanconi syndrome.

F. Manz, H. Bickel, 1989, Progress in clinical and biological research.

THE GENETICS OF LIGNAC‐FANCONI DISEASE

H. Harris, H. Bickel, 1952 .

Invited editorial comment: Neonatal thyroid screening

H. Bickel, D. Schönberg, M. Klett, 1984, European Journal of Pediatrics.

Neonatal thyroid screening.

H. Bickel, D. Schönberg, M. Klett, 1984, European Journal of Pediatrics.

Standardized loading test with protein for the differentiation of phenylketonuria from hyperphenylalaninaemia

P. Lutz, H. Schmidt, H. Bickel, 1982, Journal of Inherited Metabolic Disease.

In Vivo residual activities of the phenylalanine hydroxylating system in phenylketonuria and variants

P. Lutz, F. Trefz, H. W. Seyberth, 1981, Journal of Inherited Metabolic Disease.

In vivo determination of phenylalanine hydroxylase activity using heptadeutero-phenylalanine and comparison to the in vitro assay values.

P. Lutz, F. Trefz, H. Schmidt, 1978, Monographs in human genetics.

[Utilisation and metabolic behaviour of sorbitol during long-term parenteral perfusions (author's transl)].

F. Matzkies, G. Berg, H. Bickel, 1973, Deutsche Medizinische Wochenschrift.

[Metabolism and metabolic diseases].

H. Bickel, 1961, Monatsschrift fur Kinderheilkunde.

[Metabolism and metabolic diseases].

H. Bickel, 1966, Monatsschrift fur Kinderheilkunde.

Maple syrup urine disease: emergency treatment of the neonate.

P. Lutz, G. Hammersen, H. Schmidt, 1978, Monographs in human genetics.

Reconstitution of amino acid synthesis by combining spinach chloroplasts with other leaf organelles

G. Schultz, H. Bickel, Barbara Buchholz, 1979 .

[Methods of thin-layer chromatography for the identification of aminoaciduria, aminoacidemia and galactosemia].

H. Bremer, H. Bickel, W. Nützenadel, 1969, Monatsschrift fur Kinderheilkunde.

Influence of phenylalanine intake on phenylketonuria.

H. Bickel, J. Gerrard, E. M. Hickmans, 1953 .

Appendix. Paper chromatographic investigations on the urine of patients R.T. and R.R.

H. Bickel, E. M. Hickmans, 1952, Archives of disease in childhood.

Insulin Secretion after Long-Term Infusion of Xylitol

F. Matzkies, G. Berg, H. Bickel, 1973, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[Postoperative utilisation of parenterally administered carbohydrates].

H. Bünte, D. Coats, P. Misch, 1973, Deutsche medizinische Wochenschrift.

Early diagnosis and treatment of inborn errors of metabolism.

H. Bickel, 1987, Enzyme.

Differential diagnosis and treatment of hyperphenylalaninaemia.

H. Bickel, 1985, Progress in clinical and biological research.

Aminoaciduria in childhood

H. Bickel, 1952 .

Long-term development of intelligence (IQ) and EEG in 34 children with phenylketonuria treated early

H. Schmidt, J. Pietz, H. Bickel, 1988, European Journal of Pediatrics.

Influence of phenylalanine intake on phenylketonuria.

J. Gerrard, H. Bickel, E. M. Hickmans, 1953, Lancet.

The plastidic shikimate pathway and its role in the synthesis of plastoquinone-9, α-Tocopherol and phylloquinone in spinach chloroplasts

G. Schultz, J. Soll, H. Bickel, 1981 .