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Disk Electrophoresis of Acid Mucopolysaccharides

Nature (London), 1967-01, Vol.213 (5081), p.1133-1133

RENNERT, O. M

1967

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Metronidazole: Long Term Therapy for Methylmalonic Acidemia? 742

Pediatric research, 1998-04, Vol.43, p.129-129

1998

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Identification of three novel mutations in the acid sphingomyelinase gene of Japanese patients with Niemann-Pick disease type A and B

Human mutation, 1996, Vol.7 (1), p.65-67

1996

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Classics in Endocrinology

The Endocrinologist (Baltimore, Md.), 1995-09, Vol.5 (5), p.329

Rennert, Owen M.

1995

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Pregnancy-specific β1 glycoprotein mRNA is present in placental as well as non-placental tissues

Human reproduction (Oxford), 1988-07, Vol.3 (5), p.677-685

1988

Volltextzugriff (PDF)

Luteinizing Hormone Receptor Mutations in Disorders of Sexual Development and Cancer

Fetal and pediatric pathology, 2000, Vol.19 (1), p.21-40

2000

Volltextzugriff (PDF)

Turner Syndrome: Molecular and Cytogenetics, Dysmorphology, Endocrine, and Other Clinical Manifestations and Their Management

The Endocrinologist (Baltimore, Md.), 1994-11, Vol.4 (6), p.442-453

1994

Volltextzugriff (PDF)

COMPARISON OF COLLAGEN FROM CULTURED HUMAN FIBROBLASTS DERIVED FROM NORMAL INDIVIDUALS AND THOSE WITH CONNECTIVE TISSUE DISORDERS

Pediatric research, 1977-04, Vol.11 (4), p.455-455

1977

Volltextzugriff (PDF)

Antiprotease activity in amniotic fluid in a family with a1 antitrypsin deficiency (a1-AT)

Pediatric research, 1974-11, Vol.8 (11), p.905-905

1974

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Case Report: Dominantly Inherited Childhood Gigantism Resembling Sotos’ Syndrome

The American journal of the medical sciences, 1989-03, Vol.297 (3), p.181-185

1989

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CYSTIC-FIBROSIS FACTOR AND METACHROMASIA OF CULTURED CYSTIC-FIBROSIS FIBROBLAST

The Lancet (British edition), 1973-11, Vol.302 (7837), p.1091-1092

1973

Volltextzugriff (PDF)

a1-Antitrypsin-Mangel: Kombination von Lungenemphysem und Lebercirrhose im fr hen Kindesalter

Klinische Wochenschrift, 1975-02, Vol.53 (3), p.117-124

1975

Volltextzugriff (PDF)

500 CALCEMIC AND CALCIOTROPIC HORMONE RESPONSES TO GLUCOSE INGESTION IN NEONATES: LOWERED SERUM CA, MG, P AND ELEVATED SERUM PARATHYROID HORMONE (PTH)

Pediatric research, 1985-04, Vol.19 (4), p.194-194A

1985

Volltextzugriff (PDF)

423 BLOOD POLYAMINE DETERMINATIONS IN CHILDREN WITH LIVER DAMAGE

Pediatric research, 1978-04, Vol.12, p.434-434

1978

Volltextzugriff (PDF)

DEFECTIVE METALLOTHIONEIN IN KINKY HAIR SYNDROME FIBROBLASTS

Pediatric research, 1977-04, Vol.11 (4), p.453-453

1977

Volltextzugriff (PDF)

Antiprotease activity in tears and nasal secretions

Human genetics, 1974-03, Vol.23 (1), p.73-77

1974

Volltextzugriff (PDF)

DIFFERING POLYAMINE RESPONSES DURING TERATOGENESIS WITH DIPHENYLHYDANTOIN AND FOLIC ACID ANTAGONIST

Pediatric research, 1977-04, Vol.11 (4), p.528-528

1977

Volltextzugriff (PDF)

A variant of the cerebro-oculo-facio-skeletal syndrome with congenital ectropion and a case of lamellar ichthyosis in the same family

Clinical genetics, 1994, Vol.45 (3), p.162-163

1994

Volltextzugriff (PDF)

PLASMA INFUSION IN MENKES SYNDROME

Pediatric research, 1977-04, Vol.11 (4), p.455-455

1977

Volltextzugriff (PDF)

TRICHO-RHINO-PHALANGEAL (TRP) SYNDROME: VARYING EX- PRESSIVITY AND PROGRESSION OF SKELETAL ABNORMALITIES

Pediatric research, 1977-04, Vol.11 (4), p.525-525

1977

Volltextzugriff (PDF)

Inherent hyporesponsiveness to methylxanthine-induced behavioral changes associated with supersensitivity to 5'-N-ethylcarboxamido adenosine (NECA)

Pharmacology, biochemistry and behavior, 1986-01, Vol.25 (6), p.1271-1277

1986

Volltextzugriff (PDF)

Studies of amniotic fluid and cord blood in an infant with alpha1-antitrypsin deficiency

Human genetics, 1974, Vol.25 (3), p.241-245

1974

Volltextzugriff (PDF)

The Sanfilippo Syndrome: An Unusual Disorder of Mucopolysaccharide Metabolism

Developmental medicine and child neurology, 1970-02, Vol.12 (1), p.116-117

1970

Volltextzugriff (PDF)

Linking bonefish (Albula vulpes) populations to nearshore estuarine habitats using an otolith microchemistry approach

Environmental biology of fishes, 2019-02, Vol.102 (2), p.267-283

2019

Volltextzugriff (PDF)

Spleen phenotype in autosomal dominant polycystic kidney disease

Clinical radiology, 2019-12, Vol.74 (12), p.975.e17-975.e24

2019

Volltextzugriff (PDF)

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Disk Electrophoresis of Acid Mucopolysaccharides

Metronidazole: Long Term Therapy for Methylmalonic Acidemia? 742

Identification of three novel mutations in the acid sphingomyelinase gene of Japanese patients with Niemann-Pick disease type A and B

Classics in Endocrinology

Pregnancy-specific β1 glycoprotein mRNA is present in placental as well as non-placental tissues

Luteinizing Hormone Receptor Mutations in Disorders of Sexual Development and Cancer

Turner Syndrome: Molecular and Cytogenetics, Dysmorphology, Endocrine, and Other Clinical Manifestations and Their Management

COMPARISON OF COLLAGEN FROM CULTURED HUMAN FIBROBLASTS DERIVED FROM NORMAL INDIVIDUALS AND THOSE WITH CONNECTIVE TISSUE DISORDERS

Antiprotease activity in amniotic fluid in a family with a1 antitrypsin deficiency (a1-AT)

Case Report: Dominantly Inherited Childhood Gigantism Resembling Sotos’ Syndrome

CYSTIC-FIBROSIS FACTOR AND METACHROMASIA OF CULTURED CYSTIC-FIBROSIS FIBROBLAST

a1-Antitrypsin-Mangel: Kombination von Lungenemphysem und Lebercirrhose im fr hen Kindesalter

500 CALCEMIC AND CALCIOTROPIC HORMONE RESPONSES TO GLUCOSE INGESTION IN NEONATES: LOWERED SERUM CA, MG, P AND ELEVATED SERUM PARATHYROID HORMONE (PTH)

423 BLOOD POLYAMINE DETERMINATIONS IN CHILDREN WITH LIVER DAMAGE

DEFECTIVE METALLOTHIONEIN IN KINKY HAIR SYNDROME FIBROBLASTS

Antiprotease activity in tears and nasal secretions

DIFFERING POLYAMINE RESPONSES DURING TERATOGENESIS WITH DIPHENYLHYDANTOIN AND FOLIC ACID ANTAGONIST

A variant of the cerebro-oculo-facio-skeletal syndrome with congenital ectropion and a case of lamellar ichthyosis in the same family

PLASMA INFUSION IN MENKES SYNDROME

TRICHO-RHINO-PHALANGEAL (TRP) SYNDROME: VARYING EX- PRESSIVITY AND PROGRESSION OF SKELETAL ABNORMALITIES

Inherent hyporesponsiveness to methylxanthine-induced behavioral changes associated with supersensitivity to 5'-N-ethylcarboxamido adenosine (NECA)

Studies of amniotic fluid and cord blood in an infant with alpha1-antitrypsin deficiency

The Sanfilippo Syndrome: An Unusual Disorder of Mucopolysaccharide Metabolism

Linking bonefish (Albula vulpes) populations to nearshore estuarine habitats using an otolith microchemistry approach

Spleen phenotype in autosomal dominant polycystic kidney disease

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