cystine and Nanism

cystine has been researched along with Nanism in 24 studies

Research

Studies (24)

TimeframeStudies, this research(%)All Research%
pre-199022 (91.67)18.7374
1990's1 (4.17)18.2507
2000's0 (0.00)29.6817
2010's1 (4.17)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Besbas, N; Bilginer, Y; Gultekingil Keser, A; Topaloglu, R1
BICKEL, H1
SCHWARZ, W1
FANCONI, G; PARKER, WS; PRADER, A1
COGAN, DG; KINOSHITA, J; KUWABARA, T; RING, H; SUDARSKY, D1
HOO, LK1
LECOMTE-RAMIOUL, S1
SCHIAVINI, CA2
BRUNEAU, Y; GRISLAIN, JR; KERNEIS, JB; LEMOINE, P1
BICKEL, H; SCHMIDT, H; SPIESS, H1
SAUTER, EK1
PFANDLER, U1
DORITIS, C; PAUL, JR; SKINNER, W1
KRETCHMER, N1
SCHIFF, FS1
ALGAN, B; CORDIER, J; THOMAS, C1
STAVE, U1
BAKX, CJ1
ULLRICH, O1
Beemer, FA; Boom, BW; Kleijer, WJ1
Chapman, S1
Bradley, K; Schneider, JA; Seegmiller, JE; Wong, V1
Christensen, MF; Henriksen, O; Nielsen, JA1

Other Studies

24 other study(ies) available for cystine and Nanism

ArticleYear
Long-term endocrinologic complications of cystinosis.
    Minerva pediatrica, 2014, Volume: 66, Issue:2

    Topics: Adolescent; Adult; Biomarkers; Child; Child, Preschool; Cystine; Cystinosis; Diabetes Mellitus; Dwarfism; Female; Follow-Up Studies; Glucose Intolerance; Hospitals, University; Humans; Hypothyroidism; Male; Puberty, Delayed; Retrospective Studies; Time Factors

2014
Cystine storage disease with aminoaciduria and dwarfism; Lignac-Fanconi disease.
    Acta paediatrica, 1953, Volume: 42, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Cystine; Cystinosis; Dwarfism; Fanconi Syndrome; Metabolic Diseases; Urine

1953
[Cystinosis with aminoaciduria and nanism].
    Minerva pediatrica, 1954, Jan-15, Volume: 6, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Body Fluids; Cystine; Cystinosis; Dwarfism; Metabolic Diseases

1954
Further observations on cystine storage disease.
    Pediatrics, 1955, Volume: 16, Issue:2

    Topics: Child; Cystine; Cystinosis; Dwarfism; Humans; Infant; Metabolic Diseases

1955
Ocular manifestations of systemic cystinosis.
    A.M.A. archives of ophthalmology, 1956, Volume: 55, Issue:1

    Topics: Conjunctiva; Cornea; Cystine; Cystinosis; Dwarfism; Eye; Humans; Metabolic Diseases

1956
[Contribution to Lignac-Fanconi disease or Debré-de Toni-Fanconi syndrome].
    Maandschrift voor kindergeneeskunde, 1956, Volume: 24, Issue:2

    Topics: Cystine; Dwarfism; Fanconi Syndrome; Humans; Metabolic Diseases

1956
[A new case of cystinosis (Lignac's disease)].
    Acta paediatrica Belgica, 1955, Volume: 9, Issue:5

    Topics: Cystine; Cystinosis; Dwarfism; Metabolic Diseases

1955
[Cystinuria, cystinosis and De Toni-Debré-Fanconi disease].
    Minerva pediatrica, 1956, Apr-14, Volume: 8, Issue:15

    Topics: Cystine; Cystinosis; Cystinuria; Diagnosis, Differential; Dwarfism; Humans; Metabolic Diseases

1956
[Cystinuria, cystinosis, and De Toni-Debré-Fanconi disease].
    Pediatrie, 1956, Volume: 11, Issue:2

    Topics: Cystine; Cystinosis; Cystinuria; Dwarfism; Fanconi Syndrome; Metabolic Diseases

1956
[Pre-renal stage of cystinosis].
    Archives francaises de pediatrie, 1956, Volume: 13, Issue:4

    Topics: Cystine; Cystinosis; Dwarfism; Humans; Kidney

1956
Renal dwarfism with bone deformities in 3 siblings.
    Archiv fur Kinderheilkunde, 1956, Volume: 154, Issue:1

    Topics: Cystine; Dwarfism; Heredity; Medical Records; Metabolic Diseases

1956
[Cystinosis in infancy; clinical observations].
    Die Medizinische, 1956, Nov-24, Volume: 1, Issue:47

    Topics: Cystine; Cystinosis; Dwarfism; Metabolic Diseases

1956
The heterozygous and homozygous manifestation of certain metabolic disorders; chronic porphyria, cystinosis, Niemann-Pick disease.
    Journal de genetique humaine, 1956, Volume: 5, Issue:3-4

    Topics: Cystine; Dwarfism; Heredity; Lipidoses; Metabolic Diseases; Porphyrias

1956
Amino-aciduria in childhood: cystinuria or cystinosis?; a case report.
    Journal of the South Carolina Medical Association, 1957, Volume: 53, Issue:6

    Topics: Amino Acids; Child; Cystine; Cystinosis; Cystinuria; Dwarfism; Humans; Infant; Medical Records; Metabolic Diseases

1957
Clinical conference; cystinosis.
    Pediatrics, 1957, Volume: 19, Issue:5

    Topics: Cystine; Cystinosis; Dwarfism; Medical Records; Metabolic Diseases

1957
Cystine deposits of cornea and conjunctiva.
    A.M.A. archives of ophthalmology, 1955, Volume: 53, Issue:3

    Topics: Child; Conjunctiva; Cornea; Cystine; Dwarfism; Humans; Infant; Metabolic Diseases

1955
[Ophthalmological contributions to the diagnosis of dwarfism: cystinosis of the cornea].
    Bulletin des societes d'ophtalmologie de France, 1954, Volume: 6

    Topics: Cornea; Corneal Diseases; Cystine; Cystinosis; Disease; Dwarfism; Metabolic Diseases

1954
[Comparative amino acid studies with the aid of roentgenography and paper chromatography in the spleen in cystine storage disorder].
    Klinische Wochenschrift, 1955, Jun-15, Volume: 33, Issue:23-24

    Topics: Amino Acids; Child; Chromatography; Chromatography, Paper; Cystine; Dwarfism; Humans; Infant; Metabolic Diseases; Metabolism, Inborn Errors; Spleen

1955
[Renal rickets, renal diabetes and cystine metabolism; the De Toni-Fanconi-Debré syndrome].
    Nederlands tijdschrift voor geneeskunde, 1950, Aug-12, Volume: 94, Issue:32

    Topics: Chronic Kidney Disease-Mineral and Bone Disorder; Cystine; Diabetes Mellitus; Dwarfism; Fanconi Syndrome; Humans

1950
To the clinic and genetic biology of cystine diathesis as a major disorder in renal dwarfism and renal rickets.
    Zeitschrift fur Kinderheilkunde, 1949, Volume: 66, Issue:1-2

    Topics: Cysteine; Cystine; Dwarfism; Humans; Kidney

1949
Intermittent hair loss in a child with PIBI(D)S syndrome and trichothiodystrophy with defective DNA repair-xeroderma pigmentosum group D.
    American journal of medical genetics, 1994, Aug-15, Volume: 52, Issue:2

    Topics: Alopecia; Child, Preschool; Cystine; DNA Repair; Dwarfism; Fatal Outcome; Female; Hair; Humans; Ichthyosis; Infant, Newborn; Intellectual Disability; Recurrence; Respiratory Tract Infections; Sudden Infant Death; Syndrome; Xeroderma Pigmentosum

1994
The trichothiodystrophy syndrome of Pollitt.
    Pediatric radiology, 1988, Volume: 18, Issue:2

    Topics: Bone Diseases, Metabolic; Child, Preschool; Cystine; Dwarfism; Hair; Humans; Intellectual Disability; Male; Osteosclerosis; Syndrome

1988
Biochemical comparisons of the adult and childhood forms of cystinosis.
    The New England journal of medicine, 1968, Dec-05, Volume: 279, Issue:23

    Topics: Age Factors; Child; Culture Techniques; Cystine; Cystinosis; Dwarfism; Eye Manifestations; Female; Fibroblasts; Heterozygote; Histocytochemistry; Homozygote; Humans; Kidney Glomerulus; Kidney Tubules; Leukocytes; Male; Microscopy, Phase-Contrast; Middle Aged; Pigmentation

1968
Treatment of cystinosis with a diet poor in cystine and methionine.
    Acta paediatrica Scandinavica, 1970, Volume: 59, Issue:6

    Topics: Amino Acids; Body Height; Body Weight; Child; Child, Preschool; Cysteine; Cystine; Cystinosis; Cystinuria; Diet Therapy; Dwarfism; Ergocalciferols; Female; Humans; Ketoglutaric Acids; Male; Methionine; Pedigree; Penicillamine; Pyruvates; Renal Tubular Transport, Inborn Errors

1970